Canonical Allele Identifier: CA1933464701

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104167627A= , CM000672.2:g.104167627A=	GRCh38
NC_000010.10:g.105927385A= , CM000672.1:g.105927385A=	GRCh37
NC_000010.9:g.105917375A=	NCBI36
NG_051581.1:g.69751T=

Transcript Alleles

HGVS	Amino-acid Change
NM_025145.7:c.2802T= MANE Select	NP_079421.5:p.Cys934=
ENST00000357060.8:c.2802T= MANE Select	ENSP00000349568.3:p.Cys934=
NM_025145.5:c.2802T=	NP_079421.5:p.Cys934=
NM_025145.6:c.2802T=	NP_079421.5:p.Cys934=
ENST00000278064.6:c.2595T=	ENSP00000278064.2:p.Cys865=
ENST00000278064.7:c.2805T=	ENSP00000278064.3:p.Cys935=
ENST00000357060.7:c.2802T=	ENSP00000349568.3:p.Cys934=
ENST00000434629.5:c.884T=
XM_005270171.1:c.2805T=	XP_005270228.1:p.Cys935=
XM_005270171.2:c.2805T=	XP_005270228.1:p.Cys935=
XM_005270172.2:c.2805T=	XP_005270229.1:p.Cys935=
XM_005270172.3:c.2805T=	XP_005270229.1:p.Cys935=
XM_011540196.1:c.2919T=	XP_011538498.1:p.Cys973=
XM_011540196.2:c.2919T=	XP_011538498.1:p.Cys973=
XM_011540197.1:c.2919T=	XP_011538499.1:p.Cys973=
XM_011540197.2:c.2919T=	XP_011538499.1:p.Cys973=
XM_011540198.1:c.2802T=	XP_011538500.1:p.Cys934=
XM_011540198.2:c.2802T=	XP_011538500.1:p.Cys934=
XM_011540199.1:c.2809-909T=	XP_011538501.1:n.2809-909T=
XM_011540199.2:c.2809-909T=	XP_011538501.1:n.2809-909T=
XM_011540200.1:c.2919T=	XP_011538502.1:p.Cys973=
XM_011540200.2:c.2919T=	XP_011538502.1:p.Cys973=
XM_011540201.1:c.2919T=	XP_011538503.1:p.Cys973=
XM_011540201.2:c.2919T=	XP_011538503.1:p.Cys973=
XM_011540202.1:c.2148T=	XP_011538504.1:p.Cys716=
XM_011540202.2:c.2148T=	XP_011538504.1:p.Cys716=
XM_011540203.1:c.702T=	XP_011538505.1:p.Cys234=
XM_017016681.1:c.2916T=	XP_016872170.1:p.Cys972=
XM_017016682.1:c.2578-909T=	XP_016872171.1:n.2578-909T=
XM_017016684.1:c.2805T=	XP_016872173.1:p.Cys935=
XM_024448177.1:c.1305T=	XP_024303945.1:p.Cys435=
XM_024448178.1:c.702T=	XP_024303946.1:p.Cys234=
XR_002957015.1:n.2688T=