Canonical Allele Identifier: CA490496085

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58971387T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679188T>C , CM000677.2:g.58679188T>C	GRCh38
NC_000015.9:g.58971387T>C , CM000677.1:g.58971387T>C	GRCh37
NC_000015.8:g.56758679T>C	NCBI36
NG_033876.1:g.75791A>G
NG_033876.2:g.75520A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.420A>G MANE Select	ENSP00000260408.3:p.Ala140=
ENST00000260408.7:c.420A>G	ENSP00000260408.3:p.Ala140=
ENST00000396136.6:c.95A>G
ENST00000402627.5:c.56-38358A>G	ENSP00000386056.1:n.56-38358A>G
ENST00000439637.5:c.325+3008A>G	ENSP00000391930.1:n.325+3008A>G
ENST00000497846.5:n.537A>G
ENST00000558004.1:c.332-13991A>G	ENSP00000452704.1:n.332-13991A>G
ENST00000558733.5:n.656A>G
ENST00000559053.1:c.56-38358A>G	ENSP00000453952.1:n.56-38358A>G
ENST00000560608.5:n.558A>G
ENST00000561288.1:c.55+70292A>G	ENSP00000452639.1:n.55+70292A>G
NM_001110.3:c.420A>G	NP_001101.1:p.Ala140=
XM_005254117.2:c.420A>G	XP_005254174.1:p.Ala140=
NM_001320570.1:c.420A>G	NP_001307499.1:p.Ala140=
XM_024449818.1:c.198A>G	XP_024305586.1:p.Ala66=
NM_001110.4:c.420A>G MANE Select	NP_001101.1:p.Ala140=
NM_001320570.2:c.420A>G	NP_001307499.1:p.Ala140=