Canonical Allele Identifier: CA271729463

Gene: ADAM10

Linked Data

• dbSNP Id: rs267604273
• COSMIC: COSM142124
• MyVariant Identifiers: chr15:g.58957355G>A (hg19) ; chr15:g.58665156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665156G>A , CM000677.2:g.58665156G>A	GRCh38
NC_000015.9:g.58957355G>A , CM000677.1:g.58957355G>A	GRCh37
NC_000015.8:g.56744647G>A	NCBI36
NG_033876.1:g.89823C>T
NG_033876.2:g.89552C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.526C>T MANE Select	ENSP00000260408.3:p.His176Tyr
ENST00000260408.7:c.526C>T	ENSP00000260408.3:p.His176Tyr
ENST00000396136.6:c.352C>T
ENST00000402627.5:c.56-24326C>T	ENSP00000386056.1:n.56-24326C>T
ENST00000439637.5:c.367C>T	ENSP00000391930.1:p.His123Tyr
ENST00000497846.5:n.643C>T
ENST00000558733.5:n.762C>T
ENST00000559053.1:c.56-24326C>T	ENSP00000453952.1:n.56-24326C>T
ENST00000561288.1:c.56-67638C>T	ENSP00000452639.1:n.56-67638C>T
NM_001110.3:c.526C>T	NP_001101.1:p.His176Tyr
XM_005254117.2:c.526C>T	XP_005254174.1:p.His176Tyr
NM_001320570.1:c.526C>T	NP_001307499.1:p.His176Tyr
XM_024449818.1:c.304C>T	XP_024305586.1:p.His102Tyr
NM_001110.4:c.526C>T MANE Select	NP_001101.1:p.His176Tyr
NM_001320570.2:c.526C>T	NP_001307499.1:p.His176Tyr