Canonical Allele Identifier: CA392615870

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913676T>A (hg19) ; chr15:g.58621477T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621477T>A , CM000677.2:g.58621477T>A	GRCh38
NC_000015.9:g.58913676T>A , CM000677.1:g.58913676T>A	GRCh37
NC_000015.8:g.56700968T>A	NCBI36
NG_033876.1:g.133502A>T
NG_033876.2:g.133231A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1505A>T MANE Select	ENSP00000260408.3:p.Gln502Leu
ENST00000260408.7:c.1505A>T	ENSP00000260408.3:p.Gln502Leu
ENST00000396136.6:c.1331A>T
ENST00000402627.5:c.154+11838A>T	ENSP00000386056.1:n.154+11838A>T
ENST00000462061.1:n.65A>T
ENST00000470269.5:n.34A>T
ENST00000475898.1:n.530A>T
ENST00000481164.1:n.28A>T
ENST00000482945.5:n.28A>T
ENST00000561288.1:c.56-23959A>T	ENSP00000452639.1:n.56-23959A>T
NM_001110.3:c.1505A>T	NP_001101.1:p.Gln502Leu
XM_005254117.2:c.1412A>T	XP_005254174.1:p.Gln471Leu
NM_001320570.1:c.1412A>T	NP_001307499.1:p.Gln471Leu
XM_024449818.1:c.1283A>T	XP_024305586.1:p.Gln428Leu
NM_001110.4:c.1505A>T MANE Select	NP_001101.1:p.Gln502Leu
NM_001320570.2:c.1412A>T	NP_001307499.1:p.Gln471Leu