Canonical Allele Identifier: CA392623440

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58971385T>G (hg19) ; chr15:g.58679186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679186T>G , CM000677.2:g.58679186T>G	GRCh38
NC_000015.9:g.58971385T>G , CM000677.1:g.58971385T>G	GRCh37
NC_000015.8:g.56758677T>G	NCBI36
NG_033876.1:g.75793A>C
NG_033876.2:g.75522A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.422A>C MANE Select	ENSP00000260408.3:p.Glu141Ala
ENST00000260408.7:c.422A>C	ENSP00000260408.3:p.Glu141Ala
ENST00000396136.6:c.97A>C
ENST00000402627.5:c.56-38356A>C	ENSP00000386056.1:n.56-38356A>C
ENST00000439637.5:c.325+3010A>C	ENSP00000391930.1:n.325+3010A>C
ENST00000497846.5:n.539A>C
ENST00000558004.1:c.332-13989A>C	ENSP00000452704.1:n.332-13989A>C
ENST00000558733.5:n.658A>C
ENST00000559053.1:c.56-38356A>C	ENSP00000453952.1:n.56-38356A>C
ENST00000560608.5:n.560A>C
ENST00000561288.1:c.55+70294A>C	ENSP00000452639.1:n.55+70294A>C
NM_001110.3:c.422A>C	NP_001101.1:p.Glu141Ala
XM_005254117.2:c.422A>C	XP_005254174.1:p.Glu141Ala
NM_001320570.1:c.422A>C	NP_001307499.1:p.Glu141Ala
XM_024449818.1:c.200A>C	XP_024305586.1:p.Glu67Ala
NM_001110.4:c.422A>C MANE Select	NP_001101.1:p.Glu141Ala
NM_001320570.2:c.422A>C	NP_001307499.1:p.Glu141Ala