Canonical Allele Identifier: CA714365598

Gene: ADAM10

Linked Data

• dbSNP Id: rs572600949
• MyVariant Identifiers: chr15:g.58913587T>C (hg19) ; chr15:g.58621388T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621388T>C , CM000677.2:g.58621388T>C	GRCh38
NC_000015.9:g.58913587T>C , CM000677.1:g.58913587T>C	GRCh37
NC_000015.8:g.56700879T>C	NCBI36
NG_033876.1:g.133591A>G
NG_033876.2:g.133320A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+83A>G MANE Select	ENSP00000260408.3:n.1511+83A>G
ENST00000260408.7:c.1511+83A>G	ENSP00000260408.3:n.1511+83A>G
ENST00000396136.6:c.1337+83A>G
ENST00000402627.5:c.154+11927A>G	ENSP00000386056.1:n.154+11927A>G
ENST00000462061.1:n.71+83A>G
ENST00000470269.5:n.40+83A>G
ENST00000475898.1:n.536+83A>G
ENST00000481164.1:n.34+83A>G
ENST00000482945.5:n.34+83A>G
ENST00000561288.1:c.56-23870A>G	ENSP00000452639.1:n.56-23870A>G
NM_001110.3:c.1511+83A>G	NP_001101.1:n.1511+83A>G
XM_005254117.2:c.1418+83A>G	XP_005254174.1:n.1418+83A>G
NM_001320570.1:c.1418+83A>G	NP_001307499.1:n.1418+83A>G
XM_024449818.1:c.1289+83A>G	XP_024305586.1:n.1289+83A>G
NM_001110.4:c.1511+83A>G MANE Select	NP_001101.1:n.1511+83A>G
NM_001320570.2:c.1418+83A>G	NP_001307499.1:n.1418+83A>G