Canonical Allele Identifier: CA271731997

Gene: ADAM10

Linked Data

• dbSNP Id: rs546317994
• gnomAD v2: 15-58902938-A-G
• gnomAD v3: 15-58610739-A-G
• gnomAD v4: 15-58610739-A-G
• MyVariant Identifiers: chr15:g.58902938A>G (hg19) ; chr15:g.58610739A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610739A>G , CM000677.2:g.58610739A>G	GRCh38
NC_000015.9:g.58902938A>G , CM000677.1:g.58902938A>G	GRCh37
NC_000015.8:g.56690230A>G	NCBI36
NG_033876.1:g.144240T>C
NG_033876.2:g.143969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-222T>C MANE Select	ENSP00000260408.3:n.1805-222T>C
ENST00000260408.7:c.1805-222T>C	ENSP00000260408.3:n.1805-222T>C
ENST00000396136.6:c.1631-222T>C
ENST00000402627.5:c.155-13221T>C	ENSP00000386056.1:n.155-13221T>C
ENST00000470269.5:n.334-222T>C
ENST00000482945.5:n.1287T>C
ENST00000561288.1:c.56-13221T>C	ENSP00000452639.1:n.56-13221T>C
NM_001110.3:c.1805-222T>C	NP_001101.1:n.1805-222T>C
XM_005254117.2:c.1712-222T>C	XP_005254174.1:n.1712-222T>C
NM_001320570.1:c.1712-222T>C	NP_001307499.1:n.1712-222T>C
XM_024449818.1:c.1583-222T>C	XP_024305586.1:n.1583-222T>C
NM_001110.4:c.1805-222T>C MANE Select	NP_001101.1:n.1805-222T>C
NM_001320570.2:c.1712-222T>C	NP_001307499.1:n.1712-222T>C