Canonical Allele Identifier: CA1982223112

Gene: FCHSD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72959775A= , CM000673.2:g.72959775A=	GRCh38
NC_000011.9:g.72670820A= , CM000673.1:g.72670820A=	GRCh37
NC_000011.8:g.72348468A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409418.9:c.705+24313T= MANE Select	ENSP00000386722.4:n.705+24313T=
ENST00000311172.11:c.537+24313T=	ENSP00000308978.7:n.537+24313T=
ENST00000409314.5:c.705+24313T=	ENSP00000386987.1:n.705+24313T=
ENST00000409418.8:c.705+24313T=	ENSP00000386722.4:n.705+24313T=
ENST00000409853.5:c.537+24313T=	ENSP00000386314.1:n.537+24313T=
ENST00000458644.6:c.225+24313T=	ENSP00000402972.2:n.225+24313T=
NM_014824.2:c.705+24313T=	NP_055639.2:n.705+24313T=
XM_011545409.1:c.642+24313T=	XP_011543711.1:n.642+24313T=
XM_011545410.1:c.630+24313T=	XP_011543712.1:n.630+24313T=
XM_011545411.1:c.471+24313T=	XP_011543713.1:n.471+24313T=
XM_011545412.1:c.705+24313T=	XP_011543714.1:n.705+24313T=
XM_011545410.2:c.630+24313T=	XP_011543712.1:n.630+24313T=
XM_017018632.1:c.642+24313T=	XP_016874121.1:n.642+24313T=
XR_001748055.1:n.1510+24313T=
NM_014824.3:c.705+24313T= MANE Select	NP_055639.2:n.705+24313T=