Canonical Allele Identifier: CA392623432

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58971384C>A (hg19) ; chr15:g.58679185C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679185C>A , CM000677.2:g.58679185C>A	GRCh38
NC_000015.9:g.58971384C>A , CM000677.1:g.58971384C>A	GRCh37
NC_000015.8:g.56758676C>A	NCBI36
NG_033876.1:g.75794G>T
NG_033876.2:g.75523G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.423G>T MANE Select	ENSP00000260408.3:p.Glu141Asp
ENST00000260408.7:c.423G>T	ENSP00000260408.3:p.Glu141Asp
ENST00000396136.6:c.98G>T
ENST00000402627.5:c.56-38355G>T	ENSP00000386056.1:n.56-38355G>T
ENST00000439637.5:c.325+3011G>T	ENSP00000391930.1:n.325+3011G>T
ENST00000497846.5:n.540G>T
ENST00000558004.1:c.332-13988G>T	ENSP00000452704.1:n.332-13988G>T
ENST00000558733.5:n.659G>T
ENST00000559053.1:c.56-38355G>T	ENSP00000453952.1:n.56-38355G>T
ENST00000560608.5:n.561G>T
ENST00000561288.1:c.55+70295G>T	ENSP00000452639.1:n.55+70295G>T
NM_001110.3:c.423G>T	NP_001101.1:p.Glu141Asp
XM_005254117.2:c.423G>T	XP_005254174.1:p.Glu141Asp
NM_001320570.1:c.423G>T	NP_001307499.1:p.Glu141Asp
XM_024449818.1:c.201G>T	XP_024305586.1:p.Glu67Asp
NM_001110.4:c.423G>T MANE Select	NP_001101.1:p.Glu141Asp
NM_001320570.2:c.423G>T	NP_001307499.1:p.Glu141Asp