Canonical Allele Identifier: CA392623448

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58679189-G-T
• MyVariant Identifiers: chr15:g.58971388G>T (hg19) ; chr15:g.58679189G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679189G>T , CM000677.2:g.58679189G>T	GRCh38
NC_000015.9:g.58971388G>T , CM000677.1:g.58971388G>T	GRCh37
NC_000015.8:g.56758680G>T	NCBI36
NG_033876.1:g.75790C>A
NG_033876.2:g.75519C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.419C>A MANE Select	ENSP00000260408.3:p.Ala140Glu
ENST00000260408.7:c.419C>A	ENSP00000260408.3:p.Ala140Glu
ENST00000396136.6:c.94C>A
ENST00000402627.5:c.56-38359C>A	ENSP00000386056.1:n.56-38359C>A
ENST00000439637.5:c.325+3007C>A	ENSP00000391930.1:n.325+3007C>A
ENST00000497846.5:n.536C>A
ENST00000558004.1:c.332-13992C>A	ENSP00000452704.1:n.332-13992C>A
ENST00000558733.5:n.655C>A
ENST00000559053.1:c.56-38359C>A	ENSP00000453952.1:n.56-38359C>A
ENST00000560608.5:n.557C>A
ENST00000561288.1:c.55+70291C>A	ENSP00000452639.1:n.55+70291C>A
NM_001110.3:c.419C>A	NP_001101.1:p.Ala140Glu
XM_005254117.2:c.419C>A	XP_005254174.1:p.Ala140Glu
NM_001320570.1:c.419C>A	NP_001307499.1:p.Ala140Glu
XM_024449818.1:c.197C>A	XP_024305586.1:p.Ala66Glu
NM_001110.4:c.419C>A MANE Select	NP_001101.1:p.Ala140Glu
NM_001320570.2:c.419C>A	NP_001307499.1:p.Ala140Glu