Canonical Allele Identifier: CA392615860

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1510A>T MANE Select	ENSP00000260408.3:p.Ser504Cys
ENST00000260408.7:c.1510A>T	ENSP00000260408.3:p.Ser504Cys
ENST00000396136.6:c.1336A>T
ENST00000402627.5:c.154+11843A>T	ENSP00000386056.1:n.154+11843A>T
ENST00000462061.1:n.70A>T
ENST00000470269.5:n.39A>T
ENST00000475898.1:n.535A>T
ENST00000481164.1:n.33A>T
ENST00000482945.5:n.33A>T
ENST00000561288.1:c.56-23954A>T	ENSP00000452639.1:n.56-23954A>T
NM_001110.3:c.1510A>T	NP_001101.1:p.Ser504Cys
XM_005254117.2:c.1417A>T	XP_005254174.1:p.Ser473Cys
NM_001320570.1:c.1417A>T	NP_001307499.1:p.Ser473Cys
XM_024449818.1:c.1288A>T	XP_024305586.1:p.Ser430Cys
NM_001110.4:c.1510A>T MANE Select	NP_001101.1:p.Ser504Cys
NM_001320570.2:c.1417A>T	NP_001307499.1:p.Ser473Cys