Canonical Allele Identifier: CA2351043138

Gene: SPTLC3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.13048154A= , CM000682.2:g.13048154A=	GRCh38
NC_000020.10:g.13028802A= , CM000682.1:g.13028802A=	GRCh37
NC_000020.9:g.12976802A=	NCBI36
NG_053155.1:g.44176A=

Transcript Alleles

HGVS	Amino-acid Change
NM_018327.4:c.118-791A= MANE Select	NP_060797.2:n.118-791A=
ENST00000399002.7:c.118-791A= MANE Select	ENSP00000381968.2:n.118-791A=
NM_001349945.1:c.118-791A=	NP_001336874.1:n.118-791A=
NM_001349945.2:c.118-791A=	NP_001336874.1:n.118-791A=
NM_018327.2:c.118-791A=	NP_060797.2:n.118-791A=
NM_018327.3:c.118-791A=	NP_060797.2:n.118-791A=
ENST00000399002.6:c.118-791A=	ENSP00000381968.2:n.118-791A=
ENST00000434210.5:c.118-791A=	ENSP00000389749.1:n.118-791A=
ENST00000450297.1:c.37-791A=	ENSP00000409125.1:n.37-791A=
ENST00000476791.1:n.407-791A=
XM_011529278.1:c.118-791A=	XP_011527580.1:n.118-791A=
XM_011529279.1:c.118-791A=	XP_011527581.1:n.118-791A=
XM_017027922.1:c.118-791A=	XP_016883411.1:n.118-791A=
XR_001754317.1:n.175-791A=