Canonical Allele Identifier: CA378092165

Gene: CFAP43

Linked Data

• gnomAD v4: 10-104162322-T-C
• MyVariant Identifiers: chr10:g.105922080T>C (hg19) ; chr10:g.104162322T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162322T>C , CM000672.2:g.104162322T>C	GRCh38
NC_000010.10:g.105922080T>C , CM000672.1:g.105922080T>C	GRCh37
NC_000010.9:g.105912070T>C	NCBI36
NG_051581.1:g.75056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3328A>G MANE Select	ENSP00000349568.3:p.Ile1110Val
ENST00000357060.7:c.3328A>G	ENSP00000349568.3:p.Ile1110Val
ENST00000434629.5:c.1410A>G
NM_025145.5:c.3328A>G	NP_079421.5:p.Ile1110Val
XM_005270171.1:c.3331A>G	XP_005270228.1:p.Ile1111Val
XM_005270172.2:c.3331A>G	XP_005270229.1:p.Ile1111Val
XM_011540196.1:c.3445A>G	XP_011538498.1:p.Ile1149Val
XM_011540197.1:c.3445A>G	XP_011538499.1:p.Ile1149Val
XM_011540198.1:c.3328A>G	XP_011538500.1:p.Ile1110Val
XM_011540199.1:c.3328A>G	XP_011538501.1:p.Ile1110Val
XM_011540200.1:c.3445A>G	XP_011538502.1:p.Ile1149Val
XM_011540201.1:c.3445A>G	XP_011538503.1:p.Ile1149Val
XM_011540202.1:c.2674A>G	XP_011538504.1:p.Ile892Val
XM_011540203.1:c.1228A>G	XP_011538505.1:p.Ile410Val
NM_025145.6:c.3328A>G	NP_079421.5:p.Ile1110Val
XM_005270171.2:c.3331A>G	XP_005270228.1:p.Ile1111Val
XM_005270172.3:c.3331A>G	XP_005270229.1:p.Ile1111Val
XM_011540196.2:c.3445A>G	XP_011538498.1:p.Ile1149Val
XM_011540197.2:c.3445A>G	XP_011538499.1:p.Ile1149Val
XM_011540198.2:c.3328A>G	XP_011538500.1:p.Ile1110Val
XM_011540199.2:c.3328A>G	XP_011538501.1:p.Ile1110Val
XM_011540200.2:c.3445A>G	XP_011538502.1:p.Ile1149Val
XM_011540201.2:c.3445A>G	XP_011538503.1:p.Ile1149Val
XM_011540202.2:c.2674A>G	XP_011538504.1:p.Ile892Val
XM_017016681.1:c.3442A>G	XP_016872170.1:p.Ile1148Val
XM_017016682.1:c.3097A>G	XP_016872171.1:p.Ile1033Val
XM_024448177.1:c.1831A>G	XP_024303945.1:p.Ile611Val
XM_024448178.1:c.1228A>G	XP_024303946.1:p.Ile410Val
XR_002957015.1:n.3214A>G
NM_025145.7:c.3328A>G MANE Select	NP_079421.5:p.Ile1110Val