Canonical Allele Identifier: CA378091888

Gene: CFAP43

Linked Data

• MyVariant Identifiers: chr10:g.105921771A>C (hg19) ; chr10:g.104162013A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162013A>C , CM000672.2:g.104162013A>C	GRCh38
NC_000010.10:g.105921771A>C , CM000672.1:g.105921771A>C	GRCh37
NC_000010.9:g.105911761A>C	NCBI36
NG_051581.1:g.75365T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3362T>G MANE Select	ENSP00000349568.3:p.Met1121Arg
ENST00000357060.7:c.3362T>G	ENSP00000349568.3:p.Met1121Arg
ENST00000434629.5:c.1444T>G
NM_025145.5:c.3362T>G	NP_079421.5:p.Met1121Arg
XM_005270171.1:c.3365T>G	XP_005270228.1:p.Met1122Arg
XM_005270172.2:c.3365T>G	XP_005270229.1:p.Met1122Arg
XM_011540196.1:c.3479T>G	XP_011538498.1:p.Met1160Arg
XM_011540197.1:c.3479T>G	XP_011538499.1:p.Met1160Arg
XM_011540198.1:c.3362T>G	XP_011538500.1:p.Met1121Arg
XM_011540199.1:c.3362T>G	XP_011538501.1:p.Met1121Arg
XM_011540200.1:c.3479T>G	XP_011538502.1:p.Met1160Arg
XM_011540201.1:c.3479T>G	XP_011538503.1:p.Met1160Arg
XM_011540202.1:c.2708T>G	XP_011538504.1:p.Met903Arg
XM_011540203.1:c.1262T>G	XP_011538505.1:p.Met421Arg
NM_025145.6:c.3362T>G	NP_079421.5:p.Met1121Arg
XM_005270171.2:c.3365T>G	XP_005270228.1:p.Met1122Arg
XM_005270172.3:c.3365T>G	XP_005270229.1:p.Met1122Arg
XM_011540196.2:c.3479T>G	XP_011538498.1:p.Met1160Arg
XM_011540197.2:c.3479T>G	XP_011538499.1:p.Met1160Arg
XM_011540198.2:c.3362T>G	XP_011538500.1:p.Met1121Arg
XM_011540199.2:c.3362T>G	XP_011538501.1:p.Met1121Arg
XM_011540200.2:c.3479T>G	XP_011538502.1:p.Met1160Arg
XM_011540201.2:c.3479T>G	XP_011538503.1:p.Met1160Arg
XM_011540202.2:c.2708T>G	XP_011538504.1:p.Met903Arg
XM_017016681.1:c.3476T>G	XP_016872170.1:p.Met1159Arg
XM_017016682.1:c.3131T>G	XP_016872171.1:p.Met1044Arg
XM_024448177.1:c.1865T>G	XP_024303945.1:p.Met622Arg
XM_024448178.1:c.1262T>G	XP_024303946.1:p.Met421Arg
XR_002957015.1:n.3248T>G
NM_025145.7:c.3362T>G MANE Select	NP_079421.5:p.Met1121Arg