Canonical Allele Identifier: CA373306192

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075327T>G , CM000671.2:g.35075327T>G	GRCh38
NC_000009.11:g.35075324T>G , CM000671.1:g.35075324T>G	GRCh37
NC_000009.10:g.35065324T>G	NCBI36
NG_007312.1:g.9690A>C , LRG_499:g.9690A>C
NG_007887.1:g.2416A>C , LRG_657:g.2416A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1434-2A>C MANE Select	NP_004620.1:n.1434-2A>C
ENST00000378643.8:c.1434-2A>C MANE Select	ENSP00000367910.4:n.1434-2A>C
NM_004629.1:c.1434-2A>C , LRG_499t1:c.1434-2A>C	NP_004620.1:n.1434-2A>C
ENST00000378643.7:c.1434-2A>C	ENSP00000367910.3:n.1434-2A>C
ENST00000425676.5:c.*910-2A>C	ENSP00000412793.1:n.*910-2A>C
ENST00000448890.2:c.1434-2A>C	ENSP00000409607.2:n.1434-2A>C
ENST00000461149.2:n.2626-2A>C
ENST00000476212.1:n.45-895A>C
ENST00000481254.1:n.46-2A>C
ENST00000696700.1:n.2661-2A>C
ENST00000696701.1:n.1538-2A>C
ENST00000696702.1:c.*885-2A>C	ENSP00000512821.1:n.*885-2A>C
ENST00000696703.1:c.*818-2A>C	ENSP00000512822.1:n.*818-2A>C
ENST00000696706.1:n.1497-2A>C
ENST00000696707.1:n.1651-2A>C
ENST00000696708.1:c.*779-2A>C	ENSP00000512825.1:n.*779-2A>C
ENST00000696709.1:n.2025-2A>C
ENST00000696710.1:c.1434-2A>C	ENSP00000512826.1:n.1434-2A>C
ENST00000696711.1:n.3493-2A>C
ENST00000696712.1:n.1525-2A>C
ENST00000696713.1:c.1434-2A>C	ENSP00000512827.1:n.1434-2A>C
ENST00000696714.1:n.1818-2A>C
ENST00000696715.1:c.1434-2A>C	ENSP00000512828.1:n.1434-2A>C