Canonical Allele Identifier: CA1933459846

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104161975C= , CM000672.2:g.104161975C=	GRCh38
NC_000010.10:g.105921733C= , CM000672.1:g.105921733C=	GRCh37
NC_000010.9:g.105911723C=	NCBI36
NG_051581.1:g.75403G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3400G= MANE Select	ENSP00000349568.3:p.Asp1134=
ENST00000357060.7:c.3400G=	ENSP00000349568.3:p.Asp1134=
ENST00000434629.5:c.1482G=
NM_025145.5:c.3400G=	NP_079421.5:p.Asp1134=
XM_005270171.1:c.3403G=	XP_005270228.1:p.Asp1135=
XM_005270172.2:c.3403G=	XP_005270229.1:p.Asp1135=
XM_011540196.1:c.3517G=	XP_011538498.1:p.Asp1173=
XM_011540197.1:c.3517G=	XP_011538499.1:p.Asp1173=
XM_011540198.1:c.3400G=	XP_011538500.1:p.Asp1134=
XM_011540199.1:c.3400G=	XP_011538501.1:p.Asp1134=
XM_011540200.1:c.3517G=	XP_011538502.1:p.Asp1173=
XM_011540201.1:c.3517G=	XP_011538503.1:p.Asp1173=
XM_011540202.1:c.2746G=	XP_011538504.1:p.Asp916=
XM_011540203.1:c.1300G=	XP_011538505.1:p.Asp434=
NM_025145.6:c.3400G=	NP_079421.5:p.Asp1134=
XM_005270171.2:c.3403G=	XP_005270228.1:p.Asp1135=
XM_005270172.3:c.3403G=	XP_005270229.1:p.Asp1135=
XM_011540196.2:c.3517G=	XP_011538498.1:p.Asp1173=
XM_011540197.2:c.3517G=	XP_011538499.1:p.Asp1173=
XM_011540198.2:c.3400G=	XP_011538500.1:p.Asp1134=
XM_011540199.2:c.3400G=	XP_011538501.1:p.Asp1134=
XM_011540200.2:c.3517G=	XP_011538502.1:p.Asp1173=
XM_011540201.2:c.3517G=	XP_011538503.1:p.Asp1173=
XM_011540202.2:c.2746G=	XP_011538504.1:p.Asp916=
XM_017016681.1:c.3514G=	XP_016872170.1:p.Asp1172=
XM_017016682.1:c.3169G=	XP_016872171.1:p.Asp1057=
XM_024448177.1:c.1903G=	XP_024303945.1:p.Asp635=
XM_024448178.1:c.1300G=	XP_024303946.1:p.Asp434=
XR_002957015.1:n.3286G=
NM_025145.7:c.3400G= MANE Select	NP_079421.5:p.Asp1134=