Canonical Allele Identifier: CA271739425

Gene: ADAM10

Linked Data

• dbSNP Id: rs1041896747
• MyVariant Identifiers: chr15:g.58913605A>G (hg19) ; chr15:g.58621406A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621406A>G , CM000677.2:g.58621406A>G	GRCh38
NC_000015.9:g.58913605A>G , CM000677.1:g.58913605A>G	GRCh37
NC_000015.8:g.56700897A>G	NCBI36
NG_033876.1:g.133573T>C
NG_033876.2:g.133302T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+65T>C MANE Select	ENSP00000260408.3:n.1511+65T>C
ENST00000260408.7:c.1511+65T>C	ENSP00000260408.3:n.1511+65T>C
ENST00000396136.6:c.1337+65T>C
ENST00000402627.5:c.154+11909T>C	ENSP00000386056.1:n.154+11909T>C
ENST00000462061.1:n.71+65T>C
ENST00000470269.5:n.40+65T>C
ENST00000475898.1:n.536+65T>C
ENST00000481164.1:n.34+65T>C
ENST00000482945.5:n.34+65T>C
ENST00000561288.1:c.56-23888T>C	ENSP00000452639.1:n.56-23888T>C
NM_001110.3:c.1511+65T>C	NP_001101.1:n.1511+65T>C
XM_005254117.2:c.1418+65T>C	XP_005254174.1:n.1418+65T>C
NM_001320570.1:c.1418+65T>C	NP_001307499.1:n.1418+65T>C
XM_024449818.1:c.1289+65T>C	XP_024305586.1:n.1289+65T>C
NM_001110.4:c.1511+65T>C MANE Select	NP_001101.1:n.1511+65T>C
NM_001320570.2:c.1418+65T>C	NP_001307499.1:n.1418+65T>C