Canonical Allele Identifier: CA490496062

Gene: ADAM10

Linked Data

• dbSNP Id: rs483352914
• MyVariant Identifiers: chr15:g.58971378A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679179A>G , CM000677.2:g.58679179A>G	GRCh38
NC_000015.9:g.58971378A>G , CM000677.1:g.58971378A>G	GRCh37
NC_000015.8:g.56758670A>G	NCBI36
NG_033876.1:g.75800T>C
NG_033876.2:g.75529T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.429T>C MANE Select	ENSP00000260408.3:p.Tyr143=
ENST00000260408.7:c.429T>C	ENSP00000260408.3:p.Tyr143=
ENST00000396136.6:c.104T>C
ENST00000402627.5:c.56-38349T>C	ENSP00000386056.1:n.56-38349T>C
ENST00000439637.5:c.325+3017T>C	ENSP00000391930.1:n.325+3017T>C
ENST00000497846.5:n.546T>C
ENST00000558004.1:c.332-13982T>C	ENSP00000452704.1:n.332-13982T>C
ENST00000558733.5:n.665T>C
ENST00000559053.1:c.56-38349T>C	ENSP00000453952.1:n.56-38349T>C
ENST00000560608.5:n.567T>C
ENST00000561288.1:c.55+70301T>C	ENSP00000452639.1:n.55+70301T>C
NM_001110.3:c.429T>C	NP_001101.1:p.Tyr143=
XM_005254117.2:c.429T>C	XP_005254174.1:p.Tyr143=
NM_001320570.1:c.429T>C	NP_001307499.1:p.Tyr143=
XM_024449818.1:c.207T>C	XP_024305586.1:p.Tyr69=
NM_001110.4:c.429T>C MANE Select	NP_001101.1:p.Tyr143=
NM_001320570.2:c.429T>C	NP_001307499.1:p.Tyr143=