Canonical Allele Identifier: CA389592683

Gene: FANCM

Linked Data

• MyVariant Identifiers: chr14:g.45628449G>C (hg19) ; chr14:g.45159246G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159246G>C , CM000676.2:g.45159246G>C	GRCh38
NC_000014.8:g.45628449G>C , CM000676.1:g.45628449G>C	GRCh37
NC_000014.7:g.44698199G>C	NCBI36
NG_007417.1:g.28314G>C , LRG_502:g.28314G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1547G>C	ENSP00000450596.1:p.Ser516Thr
ENST00000556250.6:c.1547G>C	ENSP00000452033.2:p.Ser516Thr
ENST00000696641.1:c.1388G>C	ENSP00000512774.1:p.Ser463Thr
ENST00000696642.1:c.*358G>C	ENSP00000512775.1:n.*358G>C
ENST00000696643.1:c.1547G>C	ENSP00000512776.1:p.Ser516Thr
ENST00000696646.1:c.*358G>C	ENSP00000512777.1:n.*358G>C
ENST00000696647.1:c.1547G>C	ENSP00000512778.1:p.Ser516Thr
ENST00000696648.1:c.1547G>C	ENSP00000512779.1:p.Ser516Thr
ENST00000696649.1:c.1547G>C	ENSP00000512780.1:p.Ser516Thr
ENST00000696650.1:n.1495G>C
ENST00000696658.1:n.2097G>C
ENST00000696662.1:c.1469G>C	ENSP00000512788.1:p.Ser490Thr
ENST00000696663.1:c.364G>C
ENST00000696664.1:c.364G>C
ENST00000696675.1:c.1547G>C	ENSP00000512799.1:p.Ser516Thr
ENST00000696680.1:c.1415G>C	ENSP00000512803.1:p.Ser472Thr
ENST00000696681.1:c.*358G>C	ENSP00000512804.1:n.*358G>C
ENST00000696682.1:c.1547G>C	ENSP00000512805.1:p.Ser516Thr
ENST00000696683.1:c.364G>C
ENST00000696684.1:c.364G>C
ENST00000696685.1:c.364G>C
ENST00000267430.10:c.1547G>C MANE Select	ENSP00000267430.5:p.Ser516Thr
ENST00000267430.9:c.1547G>C	ENSP00000267430.5:p.Ser516Thr
ENST00000542564.6:c.1469G>C	ENSP00000442493.2:p.Ser490Thr
ENST00000556036.5:c.1547G>C	ENSP00000450596.1:p.Ser516Thr
ENST00000556250.5:c.302G>C	ENSP00000452033.1:p.Ser101Thr
NM_001308133.1:c.1469G>C	NP_001295062.1:p.Ser490Thr
NM_001308134.1:c.1547G>C	NP_001295063.1:p.Ser516Thr
NM_020937.2:c.1547G>C , LRG_502t1:c.1547G>C	NP_065988.1:p.Ser516Thr
NM_020937.3:c.1547G>C	NP_065988.1:p.Ser516Thr
XM_011537034.1:c.1547G>C	XP_011535336.1:p.Ser516Thr
XM_011537035.1:c.1469G>C	XP_011535337.1:p.Ser490Thr
XM_011537036.1:c.1547G>C	XP_011535338.1:p.Ser516Thr
XM_011537034.2:c.1547G>C	XP_011535336.1:p.Ser516Thr
XM_011537035.3:c.1469G>C	XP_011535337.1:p.Ser490Thr
XM_017021523.1:c.1547G>C	XP_016877012.1:p.Ser516Thr
XM_017021524.2:c.584G>C	XP_016877013.1:p.Ser195Thr
XM_017021525.2:c.362G>C	XP_016877014.1:p.Ser121Thr
XM_017021526.2:c.362G>C	XP_016877015.1:p.Ser121Thr
XM_017021527.1:c.362G>C	XP_016877016.1:p.Ser121Thr
XR_001750470.1:n.1639G>C
XR_001750471.2:n.1639G>C
XR_001750472.1:n.1639G>C
NM_020937.4:c.1547G>C MANE Select	NP_065988.1:p.Ser516Thr
NM_001308133.2:c.1469G>C	NP_001295062.1:p.Ser490Thr
NM_001308134.2:c.1547G>C	NP_001295063.1:p.Ser516Thr