Canonical Allele Identifier: CA2072525638

Gene: SFSWAP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131754997T= , CM000674.2:g.131754997T=	GRCh38
NC_000012.11:g.132239542T= , CM000674.1:g.132239542T=	GRCh37
NC_000012.10:g.130805495T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004592.4:c.1455-389T= MANE Select	NP_004583.2:n.1455-389T=
ENST00000261674.9:c.1455-389T= MANE Select	ENSP00000261674.4:n.1455-389T=
NM_001261411.1:c.1455-389T=	NP_001248340.1:n.1455-389T=
NM_001261411.2:c.1455-389T=	NP_001248340.1:n.1455-389T=
NM_004592.3:c.1455-389T=	NP_004583.2:n.1455-389T=
ENST00000261674.8:c.1455-389T=	ENSP00000261674.4:n.1455-389T=
ENST00000535236.5:n.4789-389T=
ENST00000537164.1:c.374-389T=
ENST00000538548.5:c.*1042-389T=	ENSP00000445832.1:n.*1042-389T=
ENST00000541286.5:c.1455-389T=	ENSP00000437738.1:n.1455-389T=
XM_011538653.1:c.1455-389T=	XP_011536955.1:n.1455-389T=
XM_011538654.1:c.1077-389T=	XP_011536956.1:n.1077-389T=
XM_011538654.2:c.1077-389T=	XP_011536956.1:n.1077-389T=
XM_011538655.1:c.1455-389T=	XP_011536957.1:n.1455-389T=
XM_011538655.2:c.1455-389T=	XP_011536957.1:n.1455-389T=
XM_017019798.1:c.1455-389T=	XP_016875287.1:n.1455-389T=
XM_017019799.1:c.834-389T=	XP_016875288.1:n.834-389T=
XM_024449125.1:c.1077-389T=	XP_024304893.1:n.1077-389T=
XM_024449126.1:c.1077-389T=	XP_024304894.1:n.1077-389T=