Canonical Allele Identifier: CA466092444

Gene: AOPEP FANCC

Linked Data

• MyVariant Identifiers: chr9:g.97869549G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95107267G>T , CM000671.2:g.95107267G>T	GRCh38
NC_000009.11:g.97869549G>T , CM000671.1:g.97869549G>T	GRCh37
NC_000009.10:g.96909370G>T	NCBI36
NG_011707.1:g.215443C>A , LRG_497:g.215443C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000710812.1:n.410+26487G>T (AOPEP)
ENST00000696260.1:n.2147C>A (FANCC)
ENST00000289081.8:c.1332C>A (FANCC) MANE Select	ENSP00000289081.3:p.Val444=
ENST00000375305.6:c.1332C>A (FANCC)	ENSP00000364454.1:p.Val444=
ENST00000649334.1:c.1477C>A (FANCC)	ENSP00000497735.1:n.1477C>A
ENST00000289081.7:c.1332C>A (FANCC)	ENSP00000289081.3:p.Val444=
ENST00000375305.5:c.1332C>A (FANCC)	ENSP00000364454.1:p.Val444=
ENST00000464627.5:n.659C>A (FANCC)
NM_000136.2:c.1332C>A , LRG_497t1:c.1332C>A (FANCC)	NP_000127.2:p.Val444=
NM_001243743.1:c.1332C>A (FANCC)	NP_001230672.1:p.Val444=
XM_005251802.2:c.651C>A (FANCC)	XP_005251859.1:p.Val217=
XM_006717001.1:c.1167C>A (FANCC)	XP_006717064.1:p.Val389=
XM_011518365.1:c.1332C>A (FANCC)	XP_011516667.1:p.Val444=
XM_011518367.1:c.876C>A (FANCC)	XP_011516669.1:p.Val292=
XM_011519121.1:c.2319+26487G>T (AOPEP)	XP_011517423.1:n.2319+26487G>T
XM_005251802.3:c.651C>A (FANCC)	XP_005251859.1:p.Val217=
XM_006717001.3:c.1167C>A (FANCC)	XP_006717064.1:p.Val389=
XM_011518365.3:c.1332C>A (FANCC)	XP_011516667.1:p.Val444=
XM_011518367.2:c.876C>A (FANCC)	XP_011516669.1:p.Val292=
XM_011519121.3:c.2319+26487G>T (AOPEP)	XP_011517423.1:n.2319+26487G>T
XM_017014452.2:c.876C>A (FANCC)	XP_016869941.1:p.Val292=
XM_017014453.1:c.876C>A (FANCC)	XP_016869942.1:p.Val292=
XM_017014454.1:c.711C>A (FANCC)	XP_016869943.1:p.Val237=
XM_024447451.1:c.1332C>A (FANCC)	XP_024303219.1:p.Val444=
XR_001746847.1:n.685G>T
NM_000136.3:c.1332C>A (FANCC) MANE Select	NP_000127.2:p.Val444=
NM_001243743.2:c.1332C>A (FANCC)	NP_001230672.1:p.Val444=