Canonical Allele Identifier: CA542825442

Gene: AMT

Linked Data

• dbSNP Id: rs1424348675
• gnomAD v2: 3-49459509-A-G
• gnomAD v3: 3-49422076-A-G
• gnomAD v4: 3-49422076-A-G
• MyVariant Identifiers: chr3:g.49459509A>G (hg19) ; chr3:g.49422076A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422076A>G , CM000665.2:g.49422076A>G	GRCh38
NC_000003.11:g.49459509A>G , CM000665.1:g.49459509A>G	GRCh37
NC_000003.10:g.49434513A>G	NCBI36
NG_015986.1:g.5603T>C , LRG_537:g.5603T>C
NG_033046.1:g.12249T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000273588.9:c.258+28T>C MANE Select	ENSP00000273588.3:n.258+28T>C
ENST00000395338.7:c.258+28T>C	ENSP00000378747.2:n.258+28T>C
ENST00000399379.7:c.60+285T>C	ENSP00000399943.2:n.60+285T>C
ENST00000427987.6:c.114+28T>C	ENSP00000403821.2:n.114+28T>C
ENST00000430521.2:c.91-27T>C	ENSP00000388068.2:n.91-27T>C
ENST00000462048.2:c.-101-27T>C	ENSP00000490465.1:n.-101-27T>C
ENST00000465925.6:n.277+28T>C
ENST00000473163.2:n.388T>C
ENST00000476127.6:n.135+28T>C
ENST00000476226.6:n.257+28T>C
ENST00000478594.6:n.263+28T>C
ENST00000480957.6:n.276+28T>C
ENST00000485108.6:n.388+28T>C
ENST00000487589.6:n.171+28T>C
ENST00000491800.3:n.397T>C
ENST00000493046.6:n.383T>C
ENST00000538581.6:c.114+28T>C	ENSP00000443200.2:n.114+28T>C
ENST00000635772.1:n.262+28T>C
ENST00000635808.1:c.258+28T>C	ENSP00000489620.1:n.258+28T>C
ENST00000635889.1:n.267+28T>C
ENST00000635936.1:n.250+28T>C
ENST00000636023.1:c.258+28T>C	ENSP00000489969.1:n.258+28T>C
ENST00000636070.1:c.91-27T>C	ENSP00000490160.1:n.91-27T>C
ENST00000636148.1:n.328+28T>C
ENST00000636166.1:c.496-504T>C	ENSP00000490106.1:n.496-504T>C
ENST00000636199.1:c.258+28T>C	ENSP00000490871.1:n.258+28T>C
ENST00000636204.1:n.1540+28T>C
ENST00000636461.1:c.3370+28T>C
ENST00000636522.1:c.90+285T>C	ENSP00000489758.1:n.90+285T>C
ENST00000636587.1:n.490+28T>C
ENST00000636597.1:c.258+28T>C	ENSP00000490251.1:n.258+28T>C
ENST00000636725.1:n.248+28T>C
ENST00000636803.1:n.248+28T>C
ENST00000636865.1:c.114+28T>C	ENSP00000490601.1:n.114+28T>C
ENST00000636871.1:n.201+28T>C
ENST00000636978.1:n.262+28T>C
ENST00000636991.1:n.281+28T>C
ENST00000637059.1:c.69+28T>C	ENSP00000490153.1:n.69+28T>C
ENST00000637088.1:n.3841T>C
ENST00000637114.1:n.250+28T>C
ENST00000637268.1:n.263+28T>C
ENST00000637291.1:n.266+28T>C
ENST00000637442.1:n.1753+28T>C
ENST00000637455.1:c.69+28T>C	ENSP00000489628.1:n.69+28T>C
ENST00000637457.1:n.285+28T>C
ENST00000637682.1:c.258+28T>C	ENSP00000489856.1:n.258+28T>C
ENST00000637684.1:n.360+28T>C
ENST00000637821.1:c.91-27T>C	ENSP00000490482.1:n.91-27T>C
ENST00000637914.1:n.277+28T>C
ENST00000637982.1:n.250+28T>C
ENST00000637994.1:n.268+28T>C
ENST00000638014.1:c.3039+28T>C
ENST00000638063.1:c.258+28T>C	ENSP00000489760.1:n.258+28T>C
ENST00000638079.1:c.*774+28T>C	ENSP00000490120.1:n.*774+28T>C
ENST00000638092.1:n.248+28T>C
ENST00000638115.1:c.*2019+28T>C	ENSP00000490296.1:n.*2019+28T>C
ENST00000273588.7:c.258+28T>C	ENSP00000273588.3:n.258+28T>C
ENST00000395338.6:c.258+28T>C	ENSP00000378747.2:n.258+28T>C
ENST00000399379.6:c.91-27T>C	ENSP00000399943.1:n.91-27T>C
ENST00000427987.5:c.250+28T>C
ENST00000430521.1:c.90+285T>C	ENSP00000388068.1:n.90+285T>C
ENST00000458307.6:c.258+28T>C	ENSP00000415619.2:n.258+28T>C
ENST00000462048.1:n.248-27T>C
ENST00000476226.5:n.323+28T>C
ENST00000478594.5:n.252+28T>C
ENST00000480957.5:n.266+28T>C
ENST00000485108.5:n.252+28T>C
ENST00000487589.5:n.360+28T>C
ENST00000493046.5:n.92-27T>C
ENST00000495436.5:n.348+28T>C
ENST00000498571.1:n.284T>C
ENST00000538581.5:c.90+285T>C	ENSP00000443200.1:n.90+285T>C
NM_000481.3:c.258+28T>C , LRG_537t1:c.258+28T>C	NP_000472.2:n.258+28T>C
NM_001164710.1:c.258+28T>C	NP_001158182.1:n.258+28T>C
NM_001164711.1:c.90+285T>C	NP_001158183.1:n.90+285T>C
NM_001164712.1:c.258+28T>C	NP_001158184.1:n.258+28T>C
NR_028435.1:n.472+28T>C
NM_000481.4:c.258+28T>C MANE Select	NP_000472.2:n.258+28T>C
NM_001164710.2:c.258+28T>C	NP_001158182.1:n.258+28T>C
NM_001164711.2:c.90+285T>C	NP_001158183.1:n.90+285T>C
NM_001164712.2:c.258+28T>C	NP_001158184.1:n.258+28T>C
NR_028435.2:n.267+28T>C