Canonical Allele Identifier: CA392615879

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913679T>G (hg19) ; chr15:g.58621480T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621480T>G , CM000677.2:g.58621480T>G	GRCh38
NC_000015.9:g.58913679T>G , CM000677.1:g.58913679T>G	GRCh37
NC_000015.8:g.56700971T>G	NCBI36
NG_033876.1:g.133499A>C
NG_033876.2:g.133228A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1502A>C MANE Select	ENSP00000260408.3:p.Lys501Thr
ENST00000260408.7:c.1502A>C	ENSP00000260408.3:p.Lys501Thr
ENST00000396136.6:c.1328A>C
ENST00000402627.5:c.154+11835A>C	ENSP00000386056.1:n.154+11835A>C
ENST00000462061.1:n.62A>C
ENST00000470269.5:n.31A>C
ENST00000475898.1:n.527A>C
ENST00000481164.1:n.25A>C
ENST00000482945.5:n.25A>C
ENST00000561288.1:c.56-23962A>C	ENSP00000452639.1:n.56-23962A>C
NM_001110.3:c.1502A>C	NP_001101.1:p.Lys501Thr
XM_005254117.2:c.1409A>C	XP_005254174.1:p.Lys470Thr
NM_001320570.1:c.1409A>C	NP_001307499.1:p.Lys470Thr
XM_024449818.1:c.1280A>C	XP_024305586.1:p.Lys427Thr
NM_001110.4:c.1502A>C MANE Select	NP_001101.1:p.Lys501Thr
NM_001320570.2:c.1409A>C	NP_001307499.1:p.Lys470Thr