Canonical Allele Identifier: CA1933460165

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162298_104162299delinsGT , CM000672.2:g.104162298_104162299delinsGT	GRCh38
NC_000010.10:g.105922056_105922057delinsGT , CM000672.1:g.105922056_105922057delinsGT	GRCh37
NC_000010.9:g.105912046_105912047delinsGT	NCBI36
NG_051581.1:g.75079_75080delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3333+18_3333+19delinsAC MANE Select	ENSP00000349568.3:n.3333+18_3333+19delinsAC
ENST00000357060.7:c.3333+18_3333+19delinsAC	ENSP00000349568.3:n.3333+18_3333+19delinsAC
ENST00000434629.5:c.1415+18_1415+19delinsAC
NM_025145.5:c.3333+18_3333+19delinsAC	NP_079421.5:n.3333+18_3333+19delinsAC
XM_005270171.1:c.3336+18_3336+19delinsAC	XP_005270228.1:n.3336+18_3336+19delinsAC
XM_005270172.2:c.3336+18_3336+19delinsAC	XP_005270229.1:n.3336+18_3336+19delinsAC
XM_011540196.1:c.3450+18_3450+19delinsAC	XP_011538498.1:n.3450+18_3450+19delinsAC
XM_011540197.1:c.3450+18_3450+19delinsAC	XP_011538499.1:n.3450+18_3450+19delinsAC
XM_011540198.1:c.3333+18_3333+19delinsAC	XP_011538500.1:n.3333+18_3333+19delinsAC
XM_011540199.1:c.3333+18_3333+19delinsAC	XP_011538501.1:n.3333+18_3333+19delinsAC
XM_011540200.1:c.3450+18_3450+19delinsAC	XP_011538502.1:n.3450+18_3450+19delinsAC
XM_011540201.1:c.3450+18_3450+19delinsAC	XP_011538503.1:n.3450+18_3450+19delinsAC
XM_011540202.1:c.2679+18_2679+19delinsAC	XP_011538504.1:n.2679+18_2679+19delinsAC
XM_011540203.1:c.1233+18_1233+19delinsAC	XP_011538505.1:n.1233+18_1233+19delinsAC
NM_025145.6:c.3333+18_3333+19delinsAC	NP_079421.5:n.3333+18_3333+19delinsAC
XM_005270171.2:c.3336+18_3336+19delinsAC	XP_005270228.1:n.3336+18_3336+19delinsAC
XM_005270172.3:c.3336+18_3336+19delinsAC	XP_005270229.1:n.3336+18_3336+19delinsAC
XM_011540196.2:c.3450+18_3450+19delinsAC	XP_011538498.1:n.3450+18_3450+19delinsAC
XM_011540197.2:c.3450+18_3450+19delinsAC	XP_011538499.1:n.3450+18_3450+19delinsAC
XM_011540198.2:c.3333+18_3333+19delinsAC	XP_011538500.1:n.3333+18_3333+19delinsAC
XM_011540199.2:c.3333+18_3333+19delinsAC	XP_011538501.1:n.3333+18_3333+19delinsAC
XM_011540200.2:c.3450+18_3450+19delinsAC	XP_011538502.1:n.3450+18_3450+19delinsAC
XM_011540201.2:c.3450+18_3450+19delinsAC	XP_011538503.1:n.3450+18_3450+19delinsAC
XM_011540202.2:c.2679+18_2679+19delinsAC	XP_011538504.1:n.2679+18_2679+19delinsAC
XM_017016681.1:c.3447+18_3447+19delinsAC	XP_016872170.1:n.3447+18_3447+19delinsAC
XM_017016682.1:c.3102+18_3102+19delinsAC	XP_016872171.1:n.3102+18_3102+19delinsAC
XM_024448177.1:c.1836+18_1836+19delinsAC	XP_024303945.1:n.1836+18_1836+19delinsAC
XM_024448178.1:c.1233+18_1233+19delinsAC	XP_024303946.1:n.1233+18_1233+19delinsAC
XR_002957015.1:n.3219+18_3219+19delinsAC
NM_025145.7:c.3333+18_3333+19delinsAC MANE Select	NP_079421.5:n.3333+18_3333+19delinsAC