Canonical Allele Identifier: CA392621781

Gene: ADAM10

Linked Data

• dbSNP Id: rs145518263
• gnomAD v3: 15-58665141-T-A
• gnomAD v4: 15-58665141-T-A
• MyVariant Identifiers: chr15:g.58957340T>A (hg19) ; chr15:g.58665141T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665141T>A , CM000677.2:g.58665141T>A	GRCh38
NC_000015.9:g.58957340T>A , CM000677.1:g.58957340T>A	GRCh37
NC_000015.8:g.56744632T>A	NCBI36
NG_033876.1:g.89838A>T
NG_033876.2:g.89567A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.541A>T MANE Select	ENSP00000260408.3:p.Arg181Ter
ENST00000260408.7:c.541A>T	ENSP00000260408.3:p.Arg181Ter
ENST00000396136.6:c.367A>T
ENST00000402627.5:c.56-24311A>T	ENSP00000386056.1:n.56-24311A>T
ENST00000558733.5:n.777A>T
ENST00000559053.1:c.56-24311A>T	ENSP00000453952.1:n.56-24311A>T
ENST00000561288.1:c.56-67623A>T	ENSP00000452639.1:n.56-67623A>T
NM_001110.3:c.541A>T	NP_001101.1:p.Arg181Ter
XM_005254117.2:c.541A>T	XP_005254174.1:p.Arg181Ter
NM_001320570.1:c.541A>T	NP_001307499.1:p.Arg181Ter
XM_024449818.1:c.319A>T	XP_024305586.1:p.Arg107Ter
NM_001110.4:c.541A>T MANE Select	NP_001101.1:p.Arg181Ter
NM_001320570.2:c.541A>T	NP_001307499.1:p.Arg181Ter