Canonical Allele Identifier: CA374109190

Gene: AOPEP FANCC

Linked Data

• MyVariant Identifiers: chr9:g.97897639C>G (hg19) ; chr9:g.95135357C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95135357C>G , CM000671.2:g.95135357C>G	GRCh38
NC_000009.11:g.97897639C>G , CM000671.1:g.97897639C>G	GRCh37
NC_000009.10:g.96937460C>G	NCBI36
NG_011707.1:g.187353G>C , LRG_497:g.187353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.411-11854C>G (AOPEP)
ENST00000696261.1:n.1223G>C (FANCC)
ENST00000289081.8:c.832G>C (FANCC) MANE Select	ENSP00000289081.3:p.Asp278His
ENST00000375305.6:c.832G>C (FANCC)	ENSP00000364454.1:p.Asp278His
ENST00000490972.7:c.832G>C (FANCC)	ENSP00000479931.1:p.Asp278His
ENST00000649334.1:c.977G>C (FANCC)	ENSP00000497735.1:n.977G>C
ENST00000649701.1:n.547G>C (FANCC)
ENST00000289081.7:c.832G>C (FANCC)	ENSP00000289081.3:p.Asp278His
ENST00000375305.5:c.832G>C (FANCC)	ENSP00000364454.1:p.Asp278His
ENST00000477942.5:n.187G>C (FANCC)
ENST00000480712.5:n.17G>C (FANCC)
ENST00000490972.6:c.832G>C (FANCC)	ENSP00000479931.1:p.Asp278His
NM_000136.2:c.832G>C , LRG_497t1:c.832G>C (FANCC)	NP_000127.2:p.Asp278His
NM_001243743.1:c.832G>C (FANCC)	NP_001230672.1:p.Asp278His
NM_001243744.1:c.832G>C (FANCC)	NP_001230673.1:p.Asp278His
XM_005251802.2:c.151G>C (FANCC)	XP_005251859.1:p.Asp51His
XM_006717001.1:c.667G>C (FANCC)	XP_006717064.1:p.Asp223His
XM_006717002.2:c.832G>C (FANCC)	XP_006717065.1:p.Asp278His
XM_006717004.2:c.832G>C (FANCC)	XP_006717067.1:p.Asp278His
XM_011518365.1:c.832G>C (FANCC)	XP_011516667.1:p.Asp278His
XM_011518366.1:c.832G>C (FANCC)	XP_011516668.1:p.Asp278His
XM_011518367.1:c.376G>C (FANCC)	XP_011516669.1:p.Asp126His
XM_011519121.1:c.2320-11854C>G (AOPEP)	XP_011517423.1:n.2320-11854C>G
XM_005251802.3:c.151G>C (FANCC)	XP_005251859.1:p.Asp51His
XM_006717001.3:c.667G>C (FANCC)	XP_006717064.1:p.Asp223His
XM_006717002.4:c.832G>C (FANCC)	XP_006717065.1:p.Asp278His
XM_006717004.4:c.832G>C (FANCC)	XP_006717067.1:p.Asp278His
XM_011518365.3:c.832G>C (FANCC)	XP_011516667.1:p.Asp278His
XM_011518366.3:c.832G>C (FANCC)	XP_011516668.1:p.Asp278His
XM_011518367.2:c.376G>C (FANCC)	XP_011516669.1:p.Asp126His
XM_011519121.3:c.2320-11854C>G (AOPEP)	XP_011517423.1:n.2320-11854C>G
XM_017014452.2:c.376G>C (FANCC)	XP_016869941.1:p.Asp126His
XM_017014453.1:c.376G>C (FANCC)	XP_016869942.1:p.Asp126His
XM_017014454.1:c.211G>C (FANCC)	XP_016869943.1:p.Asp71His
XM_024447451.1:c.832G>C (FANCC)	XP_024303219.1:p.Asp278His
NM_000136.3:c.832G>C (FANCC) MANE Select	NP_000127.2:p.Asp278His
NM_001243743.2:c.832G>C (FANCC)	NP_001230672.1:p.Asp278His
NM_001243744.2:c.832G>C (FANCC)	NP_001230673.1:p.Asp278His