Canonical Allele Identifier: CA714358863

Gene: ADAM10

Linked Data

• dbSNP Id: rs1165804164
• gnomAD v3: 15-58610731-T-A
• gnomAD v4: 15-58610731-T-A
• MyVariant Identifiers: chr15:g.58902930T>A (hg19) ; chr15:g.58610731T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610731T>A , CM000677.2:g.58610731T>A	GRCh38
NC_000015.9:g.58902930T>A , CM000677.1:g.58902930T>A	GRCh37
NC_000015.8:g.56690222T>A	NCBI36
NG_033876.1:g.144248A>T
NG_033876.2:g.143977A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-214A>T MANE Select	ENSP00000260408.3:n.1805-214A>T
ENST00000260408.7:c.1805-214A>T	ENSP00000260408.3:n.1805-214A>T
ENST00000396136.6:c.1631-214A>T
ENST00000402627.5:c.155-13213A>T	ENSP00000386056.1:n.155-13213A>T
ENST00000470269.5:n.334-214A>T
ENST00000482945.5:n.1295A>T
ENST00000561288.1:c.56-13213A>T	ENSP00000452639.1:n.56-13213A>T
NM_001110.3:c.1805-214A>T	NP_001101.1:n.1805-214A>T
XM_005254117.2:c.1712-214A>T	XP_005254174.1:n.1712-214A>T
NM_001320570.1:c.1712-214A>T	NP_001307499.1:n.1712-214A>T
XM_024449818.1:c.1583-214A>T	XP_024305586.1:n.1583-214A>T
NM_001110.4:c.1805-214A>T MANE Select	NP_001101.1:n.1805-214A>T
NM_001320570.2:c.1712-214A>T	NP_001307499.1:n.1712-214A>T