Canonical Allele Identifier: CA392615857

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913670C>G (hg19) ; chr15:g.58621471C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621471C>G , CM000677.2:g.58621471C>G	GRCh38
NC_000015.9:g.58913670C>G , CM000677.1:g.58913670C>G	GRCh37
NC_000015.8:g.56700962C>G	NCBI36
NG_033876.1:g.133508G>C
NG_033876.2:g.133237G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511G>C MANE Select	ENSP00000260408.3:p.Ser504Thr
ENST00000260408.7:c.1511G>C	ENSP00000260408.3:p.Ser504Thr
ENST00000396136.6:c.1337G>C
ENST00000402627.5:c.154+11844G>C	ENSP00000386056.1:n.154+11844G>C
ENST00000462061.1:n.71G>C
ENST00000470269.5:n.40G>C
ENST00000475898.1:n.536G>C
ENST00000481164.1:n.34G>C
ENST00000482945.5:n.34G>C
ENST00000561288.1:c.56-23953G>C	ENSP00000452639.1:n.56-23953G>C
NM_001110.3:c.1511G>C	NP_001101.1:p.Ser504Thr
XM_005254117.2:c.1418G>C	XP_005254174.1:p.Ser473Thr
NM_001320570.1:c.1418G>C	NP_001307499.1:p.Ser473Thr
XM_024449818.1:c.1289G>C	XP_024305586.1:p.Ser430Thr
NM_001110.4:c.1511G>C MANE Select	NP_001101.1:p.Ser504Thr
NM_001320570.2:c.1418G>C	NP_001307499.1:p.Ser473Thr