Canonical Allele Identifier: CA392615858

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1510A>C MANE Select	ENSP00000260408.3:p.Ser504Arg
ENST00000260408.7:c.1510A>C	ENSP00000260408.3:p.Ser504Arg
ENST00000396136.6:c.1336A>C
ENST00000402627.5:c.154+11843A>C	ENSP00000386056.1:n.154+11843A>C
ENST00000462061.1:n.70A>C
ENST00000470269.5:n.39A>C
ENST00000475898.1:n.535A>C
ENST00000481164.1:n.33A>C
ENST00000482945.5:n.33A>C
ENST00000561288.1:c.56-23954A>C	ENSP00000452639.1:n.56-23954A>C
NM_001110.3:c.1510A>C	NP_001101.1:p.Ser504Arg
XM_005254117.2:c.1417A>C	XP_005254174.1:p.Ser473Arg
NM_001320570.1:c.1417A>C	NP_001307499.1:p.Ser473Arg
XM_024449818.1:c.1288A>C	XP_024305586.1:p.Ser430Arg
NM_001110.4:c.1510A>C MANE Select	NP_001101.1:p.Ser504Arg
NM_001320570.2:c.1417A>C	NP_001307499.1:p.Ser473Arg