Canonical Allele Identifier: CA392615863

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913673C>A (hg19) ; chr15:g.58621474C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621474C>A , CM000677.2:g.58621474C>A	GRCh38
NC_000015.9:g.58913673C>A , CM000677.1:g.58913673C>A	GRCh37
NC_000015.8:g.56700965C>A	NCBI36
NG_033876.1:g.133505G>T
NG_033876.2:g.133234G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1508G>T MANE Select	ENSP00000260408.3:p.Cys503Phe
ENST00000260408.7:c.1508G>T	ENSP00000260408.3:p.Cys503Phe
ENST00000396136.6:c.1334G>T
ENST00000402627.5:c.154+11841G>T	ENSP00000386056.1:n.154+11841G>T
ENST00000462061.1:n.68G>T
ENST00000470269.5:n.37G>T
ENST00000475898.1:n.533G>T
ENST00000481164.1:n.31G>T
ENST00000482945.5:n.31G>T
ENST00000561288.1:c.56-23956G>T	ENSP00000452639.1:n.56-23956G>T
NM_001110.3:c.1508G>T	NP_001101.1:p.Cys503Phe
XM_005254117.2:c.1415G>T	XP_005254174.1:p.Cys472Phe
NM_001320570.1:c.1415G>T	NP_001307499.1:p.Cys472Phe
XM_024449818.1:c.1286G>T	XP_024305586.1:p.Cys429Phe
NM_001110.4:c.1508G>T MANE Select	NP_001101.1:p.Cys503Phe
NM_001320570.2:c.1415G>T	NP_001307499.1:p.Cys472Phe