Canonical Allele Identifier: CA392615861

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913672G>C (hg19) ; chr15:g.58621473G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621473G>C , CM000677.2:g.58621473G>C	GRCh38
NC_000015.9:g.58913672G>C , CM000677.1:g.58913672G>C	GRCh37
NC_000015.8:g.56700964G>C	NCBI36
NG_033876.1:g.133506C>G
NG_033876.2:g.133235C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1509C>G MANE Select	ENSP00000260408.3:p.Cys503Trp
ENST00000260408.7:c.1509C>G	ENSP00000260408.3:p.Cys503Trp
ENST00000396136.6:c.1335C>G
ENST00000402627.5:c.154+11842C>G	ENSP00000386056.1:n.154+11842C>G
ENST00000462061.1:n.69C>G
ENST00000470269.5:n.38C>G
ENST00000475898.1:n.534C>G
ENST00000481164.1:n.32C>G
ENST00000482945.5:n.32C>G
ENST00000561288.1:c.56-23955C>G	ENSP00000452639.1:n.56-23955C>G
NM_001110.3:c.1509C>G	NP_001101.1:p.Cys503Trp
XM_005254117.2:c.1416C>G	XP_005254174.1:p.Cys472Trp
NM_001320570.1:c.1416C>G	NP_001307499.1:p.Cys472Trp
XM_024449818.1:c.1287C>G	XP_024305586.1:p.Cys429Trp
NM_001110.4:c.1509C>G MANE Select	NP_001101.1:p.Cys503Trp
NM_001320570.2:c.1416C>G	NP_001307499.1:p.Cys472Trp