Canonical Allele Identifier: CA378091764

Gene: CFAP43

Linked Data

• MyVariant Identifiers: chr10:g.105921740C>G (hg19) ; chr10:g.104161982C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104161982C>G , CM000672.2:g.104161982C>G	GRCh38
NC_000010.10:g.105921740C>G , CM000672.1:g.105921740C>G	GRCh37
NC_000010.9:g.105911730C>G	NCBI36
NG_051581.1:g.75396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3393G>C MANE Select	ENSP00000349568.3:p.Lys1131Asn
ENST00000357060.7:c.3393G>C	ENSP00000349568.3:p.Lys1131Asn
ENST00000434629.5:c.1475G>C
NM_025145.5:c.3393G>C	NP_079421.5:p.Lys1131Asn
XM_005270171.1:c.3396G>C	XP_005270228.1:p.Lys1132Asn
XM_005270172.2:c.3396G>C	XP_005270229.1:p.Lys1132Asn
XM_011540196.1:c.3510G>C	XP_011538498.1:p.Lys1170Asn
XM_011540197.1:c.3510G>C	XP_011538499.1:p.Lys1170Asn
XM_011540198.1:c.3393G>C	XP_011538500.1:p.Lys1131Asn
XM_011540199.1:c.3393G>C	XP_011538501.1:p.Lys1131Asn
XM_011540200.1:c.3510G>C	XP_011538502.1:p.Lys1170Asn
XM_011540201.1:c.3510G>C	XP_011538503.1:p.Lys1170Asn
XM_011540202.1:c.2739G>C	XP_011538504.1:p.Lys913Asn
XM_011540203.1:c.1293G>C	XP_011538505.1:p.Lys431Asn
NM_025145.6:c.3393G>C	NP_079421.5:p.Lys1131Asn
XM_005270171.2:c.3396G>C	XP_005270228.1:p.Lys1132Asn
XM_005270172.3:c.3396G>C	XP_005270229.1:p.Lys1132Asn
XM_011540196.2:c.3510G>C	XP_011538498.1:p.Lys1170Asn
XM_011540197.2:c.3510G>C	XP_011538499.1:p.Lys1170Asn
XM_011540198.2:c.3393G>C	XP_011538500.1:p.Lys1131Asn
XM_011540199.2:c.3393G>C	XP_011538501.1:p.Lys1131Asn
XM_011540200.2:c.3510G>C	XP_011538502.1:p.Lys1170Asn
XM_011540201.2:c.3510G>C	XP_011538503.1:p.Lys1170Asn
XM_011540202.2:c.2739G>C	XP_011538504.1:p.Lys913Asn
XM_017016681.1:c.3507G>C	XP_016872170.1:p.Lys1169Asn
XM_017016682.1:c.3162G>C	XP_016872171.1:p.Lys1054Asn
XM_024448177.1:c.1896G>C	XP_024303945.1:p.Lys632Asn
XM_024448178.1:c.1293G>C	XP_024303946.1:p.Lys431Asn
XR_002957015.1:n.3279G>C
NM_025145.7:c.3393G>C MANE Select	NP_079421.5:p.Lys1131Asn