Canonical Allele Identifier: CA271732001

Gene: ADAM10

Linked Data

• dbSNP Id: rs894325535
• gnomAD v2: 15-58902941-A-G
• gnomAD v3: 15-58610742-A-G
• gnomAD v4: 15-58610742-A-G
• MyVariant Identifiers: chr15:g.58902941A>G (hg19) ; chr15:g.58610742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610742A>G , CM000677.2:g.58610742A>G	GRCh38
NC_000015.9:g.58902941A>G , CM000677.1:g.58902941A>G	GRCh37
NC_000015.8:g.56690233A>G	NCBI36
NG_033876.1:g.144237T>C
NG_033876.2:g.143966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-225T>C MANE Select	ENSP00000260408.3:n.1805-225T>C
ENST00000260408.7:c.1805-225T>C	ENSP00000260408.3:n.1805-225T>C
ENST00000396136.6:c.1631-225T>C
ENST00000402627.5:c.155-13224T>C	ENSP00000386056.1:n.155-13224T>C
ENST00000470269.5:n.334-225T>C
ENST00000482945.5:n.1284T>C
ENST00000561288.1:c.56-13224T>C	ENSP00000452639.1:n.56-13224T>C
NM_001110.3:c.1805-225T>C	NP_001101.1:n.1805-225T>C
XM_005254117.2:c.1712-225T>C	XP_005254174.1:n.1712-225T>C
NM_001320570.1:c.1712-225T>C	NP_001307499.1:n.1712-225T>C
XM_024449818.1:c.1583-225T>C	XP_024305586.1:n.1583-225T>C
NM_001110.4:c.1805-225T>C MANE Select	NP_001101.1:n.1805-225T>C
NM_001320570.2:c.1712-225T>C	NP_001307499.1:n.1712-225T>C