Canonical Allele Identifier: CA378091814

Gene: CFAP43

Linked Data

• MyVariant Identifiers: chr10:g.105921754C>G (hg19) ; chr10:g.104161996C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104161996C>G , CM000672.2:g.104161996C>G	GRCh38
NC_000010.10:g.105921754C>G , CM000672.1:g.105921754C>G	GRCh37
NC_000010.9:g.105911744C>G	NCBI36
NG_051581.1:g.75382G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3379G>C MANE Select	ENSP00000349568.3:p.Val1127Leu
ENST00000357060.7:c.3379G>C	ENSP00000349568.3:p.Val1127Leu
ENST00000434629.5:c.1461G>C
NM_025145.5:c.3379G>C	NP_079421.5:p.Val1127Leu
XM_005270171.1:c.3382G>C	XP_005270228.1:p.Val1128Leu
XM_005270172.2:c.3382G>C	XP_005270229.1:p.Val1128Leu
XM_011540196.1:c.3496G>C	XP_011538498.1:p.Val1166Leu
XM_011540197.1:c.3496G>C	XP_011538499.1:p.Val1166Leu
XM_011540198.1:c.3379G>C	XP_011538500.1:p.Val1127Leu
XM_011540199.1:c.3379G>C	XP_011538501.1:p.Val1127Leu
XM_011540200.1:c.3496G>C	XP_011538502.1:p.Val1166Leu
XM_011540201.1:c.3496G>C	XP_011538503.1:p.Val1166Leu
XM_011540202.1:c.2725G>C	XP_011538504.1:p.Val909Leu
XM_011540203.1:c.1279G>C	XP_011538505.1:p.Val427Leu
NM_025145.6:c.3379G>C	NP_079421.5:p.Val1127Leu
XM_005270171.2:c.3382G>C	XP_005270228.1:p.Val1128Leu
XM_005270172.3:c.3382G>C	XP_005270229.1:p.Val1128Leu
XM_011540196.2:c.3496G>C	XP_011538498.1:p.Val1166Leu
XM_011540197.2:c.3496G>C	XP_011538499.1:p.Val1166Leu
XM_011540198.2:c.3379G>C	XP_011538500.1:p.Val1127Leu
XM_011540199.2:c.3379G>C	XP_011538501.1:p.Val1127Leu
XM_011540200.2:c.3496G>C	XP_011538502.1:p.Val1166Leu
XM_011540201.2:c.3496G>C	XP_011538503.1:p.Val1166Leu
XM_011540202.2:c.2725G>C	XP_011538504.1:p.Val909Leu
XM_017016681.1:c.3493G>C	XP_016872170.1:p.Val1165Leu
XM_017016682.1:c.3148G>C	XP_016872171.1:p.Val1050Leu
XM_024448177.1:c.1882G>C	XP_024303945.1:p.Val628Leu
XM_024448178.1:c.1279G>C	XP_024303946.1:p.Val427Leu
XR_002957015.1:n.3265G>C
NM_025145.7:c.3379G>C MANE Select	NP_079421.5:p.Val1127Leu