Canonical Allele Identifier: CA714358867

Gene: ADAM10

Linked Data

• dbSNP Id: rs1474907298
• gnomAD v4: 15-58610733-T-A
• MyVariant Identifiers: chr15:g.58902932T>A (hg19) ; chr15:g.58610733T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610733T>A , CM000677.2:g.58610733T>A	GRCh38
NC_000015.9:g.58902932T>A , CM000677.1:g.58902932T>A	GRCh37
NC_000015.8:g.56690224T>A	NCBI36
NG_033876.1:g.144246A>T
NG_033876.2:g.143975A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1805-216A>T MANE Select	ENSP00000260408.3:n.1805-216A>T
ENST00000260408.7:c.1805-216A>T	ENSP00000260408.3:n.1805-216A>T
ENST00000396136.6:c.1631-216A>T
ENST00000402627.5:c.155-13215A>T	ENSP00000386056.1:n.155-13215A>T
ENST00000470269.5:n.334-216A>T
ENST00000482945.5:n.1293A>T
ENST00000561288.1:c.56-13215A>T	ENSP00000452639.1:n.56-13215A>T
NM_001110.3:c.1805-216A>T	NP_001101.1:n.1805-216A>T
XM_005254117.2:c.1712-216A>T	XP_005254174.1:n.1712-216A>T
NM_001320570.1:c.1712-216A>T	NP_001307499.1:n.1712-216A>T
XM_024449818.1:c.1583-216A>T	XP_024305586.1:n.1583-216A>T
NM_001110.4:c.1805-216A>T MANE Select	NP_001101.1:n.1805-216A>T
NM_001320570.2:c.1712-216A>T	NP_001307499.1:n.1712-216A>T