Canonical Allele Identifier: CA1587301856

Gene: FCHSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141641157T= , CM000667.2:g.141641157T=	GRCh38
NC_000005.9:g.141020724T= , CM000667.1:g.141020724T=	GRCh37
NC_000005.8:g.141000908T=	NCBI36
NG_029678.1:g.700A=
NG_029678.2:g.700A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000435817.7:c.*341A= MANE Select	ENSP00000399259.2:n.*341A=
ENST00000435817.6:c.*341A=	ENSP00000399259.2:n.*341A=
ENST00000520747.1:n.1327A=
ENST00000522126.5:c.*971A=	ENSP00000427796.1:n.*971A=
ENST00000522783.5:c.*502A=	ENSP00000428677.1:n.*502A=
ENST00000523856.5:n.2083A=
NM_033449.2:c.*341A=	NP_258260.1:n.*341A=
XM_005268524.3:c.*341A=	XP_005268581.1:n.*341A=
XM_006714803.2:c.*341A=	XP_006714866.1:n.*341A=
XM_005268524.5:c.*341A=	XP_005268581.1:n.*341A=
XM_006714803.4:c.*341A=	XP_006714866.1:n.*341A=
XM_011537698.3:c.*427A=	XP_011536000.1:n.*427A=
XR_002956197.1:n.2733A=
XR_427781.4:n.2406A=
XR_944338.3:n.2439A=
XR_944339.3:n.2485A=
NM_033449.3:c.*341A= MANE Select	NP_258260.1:n.*341A=