Canonical Allele Identifier: CA2647253887

Gene: AMPD1

Linked Data

• gnomAD v4: 1-114684442-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684442A>C , CM000663.2:g.114684442A>C	GRCh38
NC_000001.10:g.115227063A>C , CM000663.1:g.115227063A>C	GRCh37
NC_000001.9:g.115028586A>C	NCBI36
NG_008012.1:g.16114T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.370-78T>G	ENSP00000358551.4:n.370-78T>G
ENST00000520113.7:c.382-78T>G MANE Select	ENSP00000430075.3:n.382-78T>G
ENST00000637080.1:c.385-78T>G	ENSP00000489753.1:n.385-78T>G
ENST00000639077.1:n.46+2T>G
ENST00000369538.3:c.469-78T>G	ENSP00000358551.3:n.469-78T>G
ENST00000485564.3:n.256-78T>G
ENST00000520113.6:c.481-78T>G	ENSP00000430075.2:n.481-78T>G
NM_000036.2:c.481-78T>G	NP_000027.2:n.481-78T>G
NM_001172626.1:c.469-78T>G	NP_001166097.1:n.469-78T>G
NM_000036.3:c.382-78T>G MANE Select	NP_000027.3:n.382-78T>G
NM_001172626.2:c.370-78T>G	NP_001166097.2:n.370-78T>G