Canonical Allele Identifier: CA1933460162

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162297_104162298delinsTG , CM000672.2:g.104162297_104162298delinsTG	GRCh38
NC_000010.10:g.105922055_105922056delinsTG , CM000672.1:g.105922055_105922056delinsTG	GRCh37
NC_000010.9:g.105912045_105912046delinsTG	NCBI36
NG_051581.1:g.75080_75081delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3333+19_3333+20delinsCA MANE Select	ENSP00000349568.3:n.3333+19_3333+20delinsCA
ENST00000357060.7:c.3333+19_3333+20delinsCA	ENSP00000349568.3:n.3333+19_3333+20delinsCA
ENST00000434629.5:c.1415+19_1415+20delinsCA
NM_025145.5:c.3333+19_3333+20delinsCA	NP_079421.5:n.3333+19_3333+20delinsCA
XM_005270171.1:c.3336+19_3336+20delinsCA	XP_005270228.1:n.3336+19_3336+20delinsCA
XM_005270172.2:c.3336+19_3336+20delinsCA	XP_005270229.1:n.3336+19_3336+20delinsCA
XM_011540196.1:c.3450+19_3450+20delinsCA	XP_011538498.1:n.3450+19_3450+20delinsCA
XM_011540197.1:c.3450+19_3450+20delinsCA	XP_011538499.1:n.3450+19_3450+20delinsCA
XM_011540198.1:c.3333+19_3333+20delinsCA	XP_011538500.1:n.3333+19_3333+20delinsCA
XM_011540199.1:c.3333+19_3333+20delinsCA	XP_011538501.1:n.3333+19_3333+20delinsCA
XM_011540200.1:c.3450+19_3450+20delinsCA	XP_011538502.1:n.3450+19_3450+20delinsCA
XM_011540201.1:c.3450+19_3450+20delinsCA	XP_011538503.1:n.3450+19_3450+20delinsCA
XM_011540202.1:c.2679+19_2679+20delinsCA	XP_011538504.1:n.2679+19_2679+20delinsCA
XM_011540203.1:c.1233+19_1233+20delinsCA	XP_011538505.1:n.1233+19_1233+20delinsCA
NM_025145.6:c.3333+19_3333+20delinsCA	NP_079421.5:n.3333+19_3333+20delinsCA
XM_005270171.2:c.3336+19_3336+20delinsCA	XP_005270228.1:n.3336+19_3336+20delinsCA
XM_005270172.3:c.3336+19_3336+20delinsCA	XP_005270229.1:n.3336+19_3336+20delinsCA
XM_011540196.2:c.3450+19_3450+20delinsCA	XP_011538498.1:n.3450+19_3450+20delinsCA
XM_011540197.2:c.3450+19_3450+20delinsCA	XP_011538499.1:n.3450+19_3450+20delinsCA
XM_011540198.2:c.3333+19_3333+20delinsCA	XP_011538500.1:n.3333+19_3333+20delinsCA
XM_011540199.2:c.3333+19_3333+20delinsCA	XP_011538501.1:n.3333+19_3333+20delinsCA
XM_011540200.2:c.3450+19_3450+20delinsCA	XP_011538502.1:n.3450+19_3450+20delinsCA
XM_011540201.2:c.3450+19_3450+20delinsCA	XP_011538503.1:n.3450+19_3450+20delinsCA
XM_011540202.2:c.2679+19_2679+20delinsCA	XP_011538504.1:n.2679+19_2679+20delinsCA
XM_017016681.1:c.3447+19_3447+20delinsCA	XP_016872170.1:n.3447+19_3447+20delinsCA
XM_017016682.1:c.3102+19_3102+20delinsCA	XP_016872171.1:n.3102+19_3102+20delinsCA
XM_024448177.1:c.1836+19_1836+20delinsCA	XP_024303945.1:n.1836+19_1836+20delinsCA
XM_024448178.1:c.1233+19_1233+20delinsCA	XP_024303946.1:n.1233+19_1233+20delinsCA
XR_002957015.1:n.3219+19_3219+20delinsCA
NM_025145.7:c.3333+19_3333+20delinsCA MANE Select	NP_079421.5:n.3333+19_3333+20delinsCA