Canonical Allele Identifier: CA392615871

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1505A>C MANE Select	ENSP00000260408.3:p.Gln502Pro
ENST00000260408.7:c.1505A>C	ENSP00000260408.3:p.Gln502Pro
ENST00000396136.6:c.1331A>C
ENST00000402627.5:c.154+11838A>C	ENSP00000386056.1:n.154+11838A>C
ENST00000462061.1:n.65A>C
ENST00000470269.5:n.34A>C
ENST00000475898.1:n.530A>C
ENST00000481164.1:n.28A>C
ENST00000482945.5:n.28A>C
ENST00000561288.1:c.56-23959A>C	ENSP00000452639.1:n.56-23959A>C
NM_001110.3:c.1505A>C	NP_001101.1:p.Gln502Pro
XM_005254117.2:c.1412A>C	XP_005254174.1:p.Gln471Pro
NM_001320570.1:c.1412A>C	NP_001307499.1:p.Gln471Pro
XM_024449818.1:c.1283A>C	XP_024305586.1:p.Gln428Pro
NM_001110.4:c.1505A>C MANE Select	NP_001101.1:p.Gln502Pro
NM_001320570.2:c.1412A>C	NP_001307499.1:p.Gln471Pro