Canonical Allele Identifier: CA389607993

Gene: FANCM

Linked Data

• MyVariant Identifiers: chr14:g.45654418A>T (hg19) ; chr14:g.45185215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185215A>T , CM000676.2:g.45185215A>T	GRCh38
NC_000014.8:g.45654418A>T , CM000676.1:g.45654418A>T	GRCh37
NC_000014.7:g.44724168A>T	NCBI36
NG_007417.1:g.54283A>T , LRG_502:g.54283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2728-2A>T	ENSP00000450632.2:n.2728-2A>T
ENST00000555484.2:c.294-2A>T
ENST00000556250.6:c.4309-2A>T	ENSP00000452033.2:n.4309-2A>T
ENST00000557110.2:c.294-2A>T
ENST00000696642.1:c.*3327-2A>T	ENSP00000512775.1:n.*3327-2A>T
ENST00000696644.1:n.252-2A>T
ENST00000696645.1:n.406-2A>T
ENST00000696647.1:c.4516-2A>T	ENSP00000512778.1:n.4516-2A>T
ENST00000696648.1:c.*2541-2A>T	ENSP00000512779.1:n.*2541-2A>T
ENST00000696649.1:c.4360-2A>T	ENSP00000512780.1:n.4360-2A>T
ENST00000696650.1:n.4464-2A>T
ENST00000696659.1:c.2514-2A>T
ENST00000696663.1:c.3447-2A>T
ENST00000696664.1:c.3348-2A>T
ENST00000696665.1:c.294-2A>T
ENST00000696675.1:c.*272-2A>T	ENSP00000512799.1:n.*272-2A>T
ENST00000696683.1:c.3333-2A>T
ENST00000696684.1:c.3333-2A>T
ENST00000696685.1:c.3333-2A>T
ENST00000696686.1:n.1253-2A>T
ENST00000267430.10:c.4516-2A>T MANE Select	ENSP00000267430.5:n.4516-2A>T
ENST00000267430.9:c.4516-2A>T	ENSP00000267430.5:n.4516-2A>T
ENST00000542564.6:c.4438-2A>T	ENSP00000442493.2:n.4438-2A>T
ENST00000554809.5:c.1313-2A>T
ENST00000555013.1:n.349-2A>T
ENST00000556250.5:c.3064-2A>T	ENSP00000452033.1:n.3064-2A>T
NM_001308133.1:c.4438-2A>T	NP_001295062.1:n.4438-2A>T
NM_020937.2:c.4516-2A>T , LRG_502t1:c.4516-2A>T	NP_065988.1:n.4516-2A>T
NM_020937.3:c.4516-2A>T	NP_065988.1:n.4516-2A>T
XM_011537034.1:c.4531-2A>T	XP_011535336.1:n.4531-2A>T
XM_011537035.1:c.4453-2A>T	XP_011535337.1:n.4453-2A>T
XM_011537036.1:c.4531-2A>T	XP_011535338.1:n.4531-2A>T
XM_011537037.1:c.2545-2A>T	XP_011535339.1:n.2545-2A>T
XM_011537034.2:c.4531-2A>T	XP_011535336.1:n.4531-2A>T
XM_011537035.3:c.4453-2A>T	XP_011535337.1:n.4453-2A>T
XM_011537037.3:c.2545-2A>T	XP_011535339.1:n.2545-2A>T
XM_017021523.1:c.4531-2A>T	XP_016877012.1:n.4531-2A>T
XM_017021524.2:c.3568-2A>T	XP_016877013.1:n.3568-2A>T
XM_017021525.2:c.3346-2A>T	XP_016877014.1:n.3346-2A>T
XM_017021526.2:c.3346-2A>T	XP_016877015.1:n.3346-2A>T
XM_017021527.1:c.3331-2A>T	XP_016877016.1:n.3331-2A>T
XR_001750470.1:n.4623-2A>T
XR_001750471.2:n.4608-2A>T
XR_001750472.1:n.4660-2A>T
NM_020937.4:c.4516-2A>T MANE Select	NP_065988.1:n.4516-2A>T
NM_001308133.2:c.4438-2A>T	NP_001295062.1:n.4438-2A>T