Canonical Allele Identifier: CA352791440

Gene: AMT NICN1

Linked Data

• dbSNP Id: rs1265958704
• gnomAD v2: 3-49459829-G-A
• gnomAD v4: 3-49422396-G-A
• MyVariant Identifiers: chr3:g.49459829G>A (hg19) ; chr3:g.49422396G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49422396G>A , CM000665.2:g.49422396G>A	GRCh38
NC_000003.11:g.49459829G>A , CM000665.1:g.49459829G>A	GRCh37
NC_000003.10:g.49434833G>A	NCBI36
NG_015986.1:g.5283C>T , LRG_537:g.5283C>T
NG_033046.1:g.11929C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273588.9:c.55C>T (AMT) MANE Select	ENSP00000273588.3:p.Pro19Ser
ENST00000273598.8:c.*2437C>T (NICN1) MANE Select	ENSP00000273598.4:n.*2437C>T
ENST00000395338.7:c.55C>T (AMT)	ENSP00000378747.2:p.Pro19Ser
ENST00000399379.7:c.25C>T (AMT)	ENSP00000399943.2:p.Pro9Ser
ENST00000427987.6:c.-76C>T (AMT)	ENSP00000403821.2:n.-76C>T
ENST00000430521.2:c.55C>T (AMT)	ENSP00000388068.2:p.Pro19Ser
ENST00000462048.2:c.-102+43C>T (AMT)	ENSP00000490465.1:n.-102+43C>T
ENST00000465925.6:n.74C>T (AMT)
ENST00000473163.2:n.68C>T (AMT)
ENST00000476226.6:n.68C>T (AMT)
ENST00000478594.6:n.74C>T (AMT)
ENST00000480957.6:n.73C>T (AMT)
ENST00000485108.6:n.221-125C>T
ENST00000491800.3:n.77C>T (AMT)
ENST00000493046.6:n.63C>T (AMT)
ENST00000538581.6:c.-76C>T (AMT)	ENSP00000443200.2:n.-76C>T
ENST00000635772.1:n.59C>T (AMT)
ENST00000635808.1:c.55C>T (AMT)	ENSP00000489620.1:p.Pro19Ser
ENST00000635889.1:n.78C>T (AMT)
ENST00000636023.1:c.55C>T (AMT)	ENSP00000489969.1:p.Pro19Ser
ENST00000636070.1:c.55C>T (AMT)	ENSP00000490160.1:p.Pro19Ser
ENST00000636148.1:n.36C>T (AMT)
ENST00000636166.1:c.496-824C>T	ENSP00000490106.1:n.496-824C>T
ENST00000636199.1:c.55C>T (AMT)	ENSP00000490871.1:p.Pro19Ser
ENST00000636204.1:n.1248C>T
ENST00000636461.1:c.3078C>T
ENST00000636522.1:c.55C>T (AMT)	ENSP00000489758.1:p.Pro19Ser
ENST00000636587.1:n.198C>T (AMT)
ENST00000636597.1:c.55C>T (AMT)	ENSP00000490251.1:p.Pro19Ser
ENST00000636725.1:n.59C>T (AMT)
ENST00000636803.1:n.59C>T (AMT)
ENST00000636865.1:c.-76C>T (AMT)	ENSP00000490601.1:n.-76C>T
ENST00000636978.1:n.59C>T (AMT)
ENST00000636991.1:n.78C>T (AMT)
ENST00000637088.1:n.3521C>T
ENST00000637114.1:n.47C>T (AMT)
ENST00000637268.1:n.74C>T (AMT)
ENST00000637291.1:n.63C>T (AMT)
ENST00000637442.1:n.1461C>T
ENST00000637457.1:n.96C>T (AMT)
ENST00000637682.1:c.55C>T (AMT)	ENSP00000489856.1:p.Pro19Ser
ENST00000637684.1:n.68C>T (AMT)
ENST00000637821.1:c.55C>T (AMT)	ENSP00000490482.1:p.Pro19Ser
ENST00000637914.1:n.74C>T (AMT)
ENST00000637994.1:n.65C>T (AMT)
ENST00000638014.1:c.2747C>T
ENST00000638063.1:c.55C>T (AMT)	ENSP00000489760.1:p.Pro19Ser
ENST00000638079.1:c.*607-125C>T	ENSP00000490120.1:n.*607-125C>T
ENST00000638092.1:n.59C>T (AMT)
ENST00000638115.1:c.*1852-125C>T	ENSP00000490296.1:n.*1852-125C>T
ENST00000273588.7:c.55C>T (AMT)	ENSP00000273588.3:p.Pro19Ser
ENST00000395338.6:c.55C>T (AMT)	ENSP00000378747.2:p.Pro19Ser
ENST00000399379.6:c.55C>T (AMT)	ENSP00000399943.1:p.Pro19Ser
ENST00000427987.5:c.47C>T (AMT)
ENST00000430521.1:c.55C>T (AMT)	ENSP00000388068.1:p.Pro19Ser
ENST00000458307.6:c.55C>T (AMT)	ENSP00000415619.2:p.Pro19Ser
ENST00000462048.1:n.247+43C>T (AMT)
ENST00000476226.5:n.134C>T (AMT)
ENST00000478594.5:n.63C>T (AMT)
ENST00000480957.5:n.63C>T (AMT)
ENST00000485108.5:n.63C>T (AMT)
ENST00000487589.5:n.68C>T (AMT)
ENST00000493046.5:n.56C>T (AMT)
ENST00000495436.5:n.56C>T (AMT)
ENST00000498571.1:n.53C>T (AMT)
ENST00000538581.5:c.55C>T (AMT)	ENSP00000443200.1:p.Pro19Ser
NM_000481.3:c.55C>T , LRG_537t1:c.55C>T (AMT)	NP_000472.2:p.Pro19Ser
NM_001164710.1:c.55C>T (AMT)	NP_001158182.1:p.Pro19Ser
NM_001164711.1:c.55C>T (AMT)	NP_001158183.1:p.Pro19Ser
NM_001164712.1:c.55C>T (AMT)	NP_001158184.1:p.Pro19Ser
NM_032316.3:c.*2437C>T (NICN1) MANE Select	NP_115692.1:n.*2437C>T
NR_028435.1:n.283C>T (AMT)
NM_000481.4:c.55C>T (AMT) MANE Select	NP_000472.2:p.Pro19Ser
NM_001164710.2:c.55C>T (AMT)	NP_001158182.1:p.Pro19Ser
NM_001164711.2:c.55C>T (AMT)	NP_001158183.1:p.Pro19Ser
NM_001164712.2:c.55C>T (AMT)	NP_001158184.1:p.Pro19Ser
NR_028435.2:n.78C>T (AMT)