Canonical Allele Identifier: CA392615859

Gene: ADAM10

Linked Data

• COSMIC: COSM4659252
• MyVariant Identifiers: chr15:g.58913671T>C (hg19) ; chr15:g.58621472T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621472T>C , CM000677.2:g.58621472T>C	GRCh38
NC_000015.9:g.58913671T>C , CM000677.1:g.58913671T>C	GRCh37
NC_000015.8:g.56700963T>C	NCBI36
NG_033876.1:g.133507A>G
NG_033876.2:g.133236A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1510A>G MANE Select	ENSP00000260408.3:p.Ser504Gly
ENST00000260408.7:c.1510A>G	ENSP00000260408.3:p.Ser504Gly
ENST00000396136.6:c.1336A>G
ENST00000402627.5:c.154+11843A>G	ENSP00000386056.1:n.154+11843A>G
ENST00000462061.1:n.70A>G
ENST00000470269.5:n.39A>G
ENST00000475898.1:n.535A>G
ENST00000481164.1:n.33A>G
ENST00000482945.5:n.33A>G
ENST00000561288.1:c.56-23954A>G	ENSP00000452639.1:n.56-23954A>G
NM_001110.3:c.1510A>G	NP_001101.1:p.Ser504Gly
XM_005254117.2:c.1417A>G	XP_005254174.1:p.Ser473Gly
NM_001320570.1:c.1417A>G	NP_001307499.1:p.Ser473Gly
XM_024449818.1:c.1288A>G	XP_024305586.1:p.Ser430Gly
NM_001110.4:c.1510A>G MANE Select	NP_001101.1:p.Ser504Gly
NM_001320570.2:c.1417A>G	NP_001307499.1:p.Ser473Gly