Canonical Allele Identifier: CA1933459757

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104161899_104161900delinsTA , CM000672.2:g.104161899_104161900delinsTA	GRCh38
NC_000010.10:g.105921657_105921658delinsTA , CM000672.1:g.105921657_105921658delinsTA	GRCh37
NC_000010.9:g.105911647_105911648delinsTA	NCBI36
NG_051581.1:g.75478_75479delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3414+61_3414+62delinsTA MANE Select	ENSP00000349568.3:n.3414+61_3414+62delinsTA
ENST00000357060.7:c.3414+61_3414+62delinsTA	ENSP00000349568.3:n.3414+61_3414+62delinsTA
ENST00000434629.5:c.1496+61_1496+62delinsTA
NM_025145.5:c.3414+61_3414+62delinsTA	NP_079421.5:n.3414+61_3414+62delinsTA
XM_005270171.1:c.3417+61_3417+62delinsTA	XP_005270228.1:n.3417+61_3417+62delinsTA
XM_005270172.2:c.3417+61_3417+62delinsTA	XP_005270229.1:n.3417+61_3417+62delinsTA
XM_011540196.1:c.3531+61_3531+62delinsTA	XP_011538498.1:n.3531+61_3531+62delinsTA
XM_011540197.1:c.3531+61_3531+62delinsTA	XP_011538499.1:n.3531+61_3531+62delinsTA
XM_011540198.1:c.3414+61_3414+62delinsTA	XP_011538500.1:n.3414+61_3414+62delinsTA
XM_011540199.1:c.3414+61_3414+62delinsTA	XP_011538501.1:n.3414+61_3414+62delinsTA
XM_011540200.1:c.3531+61_3531+62delinsTA	XP_011538502.1:n.3531+61_3531+62delinsTA
XM_011540201.1:c.3531+61_3531+62delinsTA	XP_011538503.1:n.3531+61_3531+62delinsTA
XM_011540202.1:c.2760+61_2760+62delinsTA	XP_011538504.1:n.2760+61_2760+62delinsTA
XM_011540203.1:c.1314+61_1314+62delinsTA	XP_011538505.1:n.1314+61_1314+62delinsTA
NM_025145.6:c.3414+61_3414+62delinsTA	NP_079421.5:n.3414+61_3414+62delinsTA
XM_005270171.2:c.3417+61_3417+62delinsTA	XP_005270228.1:n.3417+61_3417+62delinsTA
XM_005270172.3:c.3417+61_3417+62delinsTA	XP_005270229.1:n.3417+61_3417+62delinsTA
XM_011540196.2:c.3531+61_3531+62delinsTA	XP_011538498.1:n.3531+61_3531+62delinsTA
XM_011540197.2:c.3531+61_3531+62delinsTA	XP_011538499.1:n.3531+61_3531+62delinsTA
XM_011540198.2:c.3414+61_3414+62delinsTA	XP_011538500.1:n.3414+61_3414+62delinsTA
XM_011540199.2:c.3414+61_3414+62delinsTA	XP_011538501.1:n.3414+61_3414+62delinsTA
XM_011540200.2:c.3531+61_3531+62delinsTA	XP_011538502.1:n.3531+61_3531+62delinsTA
XM_011540201.2:c.3531+61_3531+62delinsTA	XP_011538503.1:n.3531+61_3531+62delinsTA
XM_011540202.2:c.2760+61_2760+62delinsTA	XP_011538504.1:n.2760+61_2760+62delinsTA
XM_017016681.1:c.3528+61_3528+62delinsTA	XP_016872170.1:n.3528+61_3528+62delinsTA
XM_017016682.1:c.3183+61_3183+62delinsTA	XP_016872171.1:n.3183+61_3183+62delinsTA
XM_024448177.1:c.1917+61_1917+62delinsTA	XP_024303945.1:n.1917+61_1917+62delinsTA
XM_024448178.1:c.1314+61_1314+62delinsTA	XP_024303946.1:n.1314+61_1314+62delinsTA
XR_002957015.1:n.3300+61_3300+62delinsTA
NM_025145.7:c.3414+61_3414+62delinsTA MANE Select	NP_079421.5:n.3414+61_3414+62delinsTA