Canonical Allele Identifier: CA1005999239

Gene: AMPD1

Linked Data

• gnomAD v3: 1-114677753-G-C
• gnomAD v4: 1-114677753-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677753G>C , CM000663.2:g.114677753G>C	GRCh38
NC_000001.10:g.115220374G>C , CM000663.1:g.115220374G>C	GRCh37
NC_000001.9:g.115021897G>C	NCBI36
NG_008012.1:g.22803C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1212+157C>G	ENSP00000358551.4:n.1212+157C>G
ENST00000520113.7:c.1224+157C>G MANE Select	ENSP00000430075.3:n.1224+157C>G
ENST00000637080.1:c.1007+157C>G	ENSP00000489753.1:n.1007+157C>G
ENST00000639077.1:n.889+157C>G
ENST00000369538.3:c.1311+157C>G	ENSP00000358551.3:n.1311+157C>G
ENST00000520113.6:c.1323+157C>G	ENSP00000430075.2:n.1323+157C>G
NM_000036.2:c.1323+157C>G	NP_000027.2:n.1323+157C>G
NM_001172626.1:c.1311+157C>G	NP_001166097.1:n.1311+157C>G
NM_000036.3:c.1224+157C>G MANE Select	NP_000027.3:n.1224+157C>G
NM_001172626.2:c.1212+157C>G	NP_001166097.2:n.1212+157C>G