Canonical Allele Identifier: CA2949470

Gene: ODAM

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70201464A>C , CM000666.2:g.70201464A>C	GRCh38
NC_000004.11:g.71067181A>C , CM000666.1:g.71067181A>C	GRCh37
NC_000004.10:g.71101770A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017855.4:c.539A>C MANE Select	NP_060325.3:p.Tyr180Ser
ENST00000683306.1:c.539A>C MANE Select	ENSP00000507531.1:p.Tyr180Ser
NM_001385579.1:c.529-794A>C	NP_001372508.1:n.529-794A>C
NM_017855.3:c.539A>C	NP_060325.3:p.Tyr180Ser
ENST00000396094.6:c.539A>C	ENSP00000379401.2:p.Tyr180Ser
ENST00000510709.6:c.497A>C	ENSP00000423070.2:p.Tyr166Ser
ENST00000510847.1:c.248A>C	ENSP00000422100.1:n.248A>C
ENST00000514097.5:c.388-794A>C	ENSP00000426106.1:n.388-794A>C
XM_005265698.2:c.590A>C	XP_005265755.1:p.Tyr197Ser
XM_005265698.3:c.590A>C	XP_005265755.1:p.Tyr197Ser
XM_006714245.2:c.580-794A>C	XP_006714308.1:n.580-794A>C
XM_006714245.4:c.580-794A>C	XP_006714308.1:n.580-794A>C
XM_011532052.1:c.548A>C	XP_011530354.1:p.Tyr183Ser
XM_017008331.1:c.497A>C	XP_016863820.1:p.Tyr166Ser