Canonical Allele Identifier: CA2690788304

Linked Data

gnomAD v4: 9-95107287-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.95107287A>C , CM000671.2:g.95107287A>C GRCh38
NC_000009.11:g.97869569A>C , CM000671.1:g.97869569A>C GRCh37
NC_000009.10:g.96909390A>C NCBI36
NG_011707.1:g.215423T>G , LRG_497:g.215423T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000710812.1:n.410+26507A>C (AOPEP)
ENST00000696260.1:n.2145-18T>G (FANCC)
ENST00000289081.8:c.1330-18T>G (FANCC) MANE Select ENSP00000289081.3:n.1330-18T>G
ENST00000375305.6:c.1330-18T>G (FANCC) ENSP00000364454.1:n.1330-18T>G
ENST00000649334.1:c.1475-18T>G (FANCC) ENSP00000497735.1:n.1475-18T>G
ENST00000289081.7:c.1330-18T>G (FANCC) ENSP00000289081.3:n.1330-18T>G
ENST00000375305.5:c.1330-18T>G (FANCC) ENSP00000364454.1:n.1330-18T>G
ENST00000464627.5:n.657-18T>G (FANCC)
NM_000136.2:c.1330-18T>G , LRG_497t1:c.1330-18T>G (FANCC) NP_000127.2:n.1330-18T>G
NM_001243743.1:c.1330-18T>G (FANCC) NP_001230672.1:n.1330-18T>G
XM_005251802.2:c.649-18T>G (FANCC) XP_005251859.1:n.649-18T>G
XM_006717001.1:c.1165-18T>G (FANCC) XP_006717064.1:n.1165-18T>G
XM_011518365.1:c.1330-18T>G (FANCC) XP_011516667.1:n.1330-18T>G
XM_011518367.1:c.874-18T>G (FANCC) XP_011516669.1:n.874-18T>G
XM_011519121.1:c.2319+26507A>C (AOPEP) XP_011517423.1:n.2319+26507A>C
XM_005251802.3:c.649-18T>G (FANCC) XP_005251859.1:n.649-18T>G
XM_006717001.3:c.1165-18T>G (FANCC) XP_006717064.1:n.1165-18T>G
XM_011518365.3:c.1330-18T>G (FANCC) XP_011516667.1:n.1330-18T>G
XM_011518367.2:c.874-18T>G (FANCC) XP_011516669.1:n.874-18T>G
XM_011519121.3:c.2319+26507A>C (AOPEP) XP_011517423.1:n.2319+26507A>C
XM_017014452.2:c.874-18T>G (FANCC) XP_016869941.1:n.874-18T>G
XM_017014453.1:c.874-18T>G (FANCC) XP_016869942.1:n.874-18T>G
XM_017014454.1:c.709-18T>G (FANCC) XP_016869943.1:n.709-18T>G
XM_024447451.1:c.1330-18T>G (FANCC) XP_024303219.1:n.1330-18T>G
XR_001746847.1:n.705A>C
NM_000136.3:c.1330-18T>G (FANCC) MANE Select NP_000127.2:n.1330-18T>G
NM_001243743.2:c.1330-18T>G (FANCC) NP_001230672.1:n.1330-18T>G