Canonical Allele Identifier: CA392623410

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58971379T>G (hg19) ; chr15:g.58679180T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679180T>G , CM000677.2:g.58679180T>G	GRCh38
NC_000015.9:g.58971379T>G , CM000677.1:g.58971379T>G	GRCh37
NC_000015.8:g.56758671T>G	NCBI36
NG_033876.1:g.75799A>C
NG_033876.2:g.75528A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.428A>C MANE Select	ENSP00000260408.3:p.Tyr143Ser
ENST00000260408.7:c.428A>C	ENSP00000260408.3:p.Tyr143Ser
ENST00000396136.6:c.103A>C
ENST00000402627.5:c.56-38350A>C	ENSP00000386056.1:n.56-38350A>C
ENST00000439637.5:c.325+3016A>C	ENSP00000391930.1:n.325+3016A>C
ENST00000497846.5:n.545A>C
ENST00000558004.1:c.332-13983A>C	ENSP00000452704.1:n.332-13983A>C
ENST00000558733.5:n.664A>C
ENST00000559053.1:c.56-38350A>C	ENSP00000453952.1:n.56-38350A>C
ENST00000560608.5:n.566A>C
ENST00000561288.1:c.55+70300A>C	ENSP00000452639.1:n.55+70300A>C
NM_001110.3:c.428A>C	NP_001101.1:p.Tyr143Ser
XM_005254117.2:c.428A>C	XP_005254174.1:p.Tyr143Ser
NM_001320570.1:c.428A>C	NP_001307499.1:p.Tyr143Ser
XM_024449818.1:c.206A>C	XP_024305586.1:p.Tyr69Ser
NM_001110.4:c.428A>C MANE Select	NP_001101.1:p.Tyr143Ser
NM_001320570.2:c.428A>C	NP_001307499.1:p.Tyr143Ser