Canonical Allele Identifier: CA1456062954

Gene: CWH43

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.49060883C= , CM000666.2:g.49060883C=	GRCh38
NC_000004.11:g.49062900C= , CM000666.1:g.49062900C=	GRCh37
NC_000004.10:g.48757657C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000226432.9:c.2022-929C= MANE Select	ENSP00000226432.4:n.2022-929C=
ENST00000226432.8:c.2022-929C=	ENSP00000226432.4:n.2022-929C=
ENST00000513409.1:c.1941-929C=	ENSP00000422802.1:n.1941-929C=
ENST00000514053.6:c.*1032-929C=	ENSP00000425157.2:n.*1032-929C=
NM_001286791.1:c.1941-929C=	NP_001273720.1:n.1941-929C=
NM_025087.2:c.2022-929C=	NP_079363.2:n.2022-929C=
XM_011513755.1:c.2079-929C=	XP_011512057.1:n.2079-929C=
XM_011513756.1:c.1998-929C=	XP_011512058.1:n.1998-929C=
XM_011513757.1:c.1998-929C=	XP_011512059.1:n.1998-929C=
XM_011513758.1:c.1821-929C=	XP_011512060.1:n.1821-929C=
XM_011513759.1:c.1515-929C=	XP_011512061.1:n.1515-929C=
XM_011513756.3:c.1998-929C=	XP_011512058.1:n.1998-929C=
XM_011513757.2:c.1998-929C=	XP_011512059.1:n.1998-929C=
NM_025087.3:c.2022-929C= MANE Select	NP_079363.2:n.2022-929C=
NM_001286791.2:c.1941-929C=	NP_001273720.1:n.1941-929C=