Canonical Allele Identifier: CA392623414

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58971380A>T (hg19) ; chr15:g.58679181A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679181A>T , CM000677.2:g.58679181A>T	GRCh38
NC_000015.9:g.58971380A>T , CM000677.1:g.58971380A>T	GRCh37
NC_000015.8:g.56758672A>T	NCBI36
NG_033876.1:g.75798T>A
NG_033876.2:g.75527T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.427T>A MANE Select	ENSP00000260408.3:p.Tyr143Asn
ENST00000260408.7:c.427T>A	ENSP00000260408.3:p.Tyr143Asn
ENST00000396136.6:c.102T>A
ENST00000402627.5:c.56-38351T>A	ENSP00000386056.1:n.56-38351T>A
ENST00000439637.5:c.325+3015T>A	ENSP00000391930.1:n.325+3015T>A
ENST00000497846.5:n.544T>A
ENST00000558004.1:c.332-13984T>A	ENSP00000452704.1:n.332-13984T>A
ENST00000558733.5:n.663T>A
ENST00000559053.1:c.56-38351T>A	ENSP00000453952.1:n.56-38351T>A
ENST00000560608.5:n.565T>A
ENST00000561288.1:c.55+70299T>A	ENSP00000452639.1:n.55+70299T>A
NM_001110.3:c.427T>A	NP_001101.1:p.Tyr143Asn
XM_005254117.2:c.427T>A	XP_005254174.1:p.Tyr143Asn
NM_001320570.1:c.427T>A	NP_001307499.1:p.Tyr143Asn
XM_024449818.1:c.205T>A	XP_024305586.1:p.Tyr69Asn
NM_001110.4:c.427T>A MANE Select	NP_001101.1:p.Tyr143Asn
NM_001320570.2:c.427T>A	NP_001307499.1:p.Tyr143Asn