Canonical Allele Identifier: CA1587301845

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141641152T= , CM000667.2:g.141641152T=	GRCh38
NC_000005.9:g.141020719T= , CM000667.1:g.141020719T=	GRCh37
NC_000005.8:g.141000903T=	NCBI36
NG_029678.1:g.705A=
NG_029678.2:g.705A=

Transcript Alleles

HGVS	Amino-acid Change
NM_033449.3:c.*346A= MANE Select	NP_258260.1:n.*346A=
ENST00000435817.7:c.*346A= MANE Select	ENSP00000399259.2:n.*346A=
NM_033449.2:c.*346A=	NP_258260.1:n.*346A=
ENST00000435817.6:c.*346A=	ENSP00000399259.2:n.*346A=
ENST00000520747.1:n.1332A=
ENST00000522126.5:c.*976A=	ENSP00000427796.1:n.*976A=
ENST00000522783.5:c.*507A=	ENSP00000428677.1:n.*507A=
ENST00000523856.5:n.2088A=
XM_005268524.3:c.*346A=	XP_005268581.1:n.*346A=
XM_005268524.5:c.*346A=	XP_005268581.1:n.*346A=
XM_006714803.2:c.*346A=	XP_006714866.1:n.*346A=
XM_006714803.4:c.*346A=	XP_006714866.1:n.*346A=
XM_011537698.3:c.*432A=	XP_011536000.1:n.*432A=
XR_002956197.1:n.2738A=
XR_427781.4:n.2411A=
XR_944338.3:n.2444A=
XR_944339.3:n.2490A=