Canonical Allele Identifier: CA2785167049

Gene: AOPEP FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95101893_95101894insAACACACCCAA , CM000671.2:g.95101893_95101894insAACACACCCAA	GRCh38
NC_000009.11:g.97864175_97864176insAACACACCCAA , CM000671.1:g.97864175_97864176insAACACACCCAA	GRCh37
NC_000009.10:g.96903996_96903997insAACACACCCAA	NCBI36
NG_011707.1:g.220817_220818insTGGGTGTGTTT , LRG_497:g.220817_220818insTGGGTGTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710812.1:n.410+21113_410+21114insAACACACCCAA (AOPEP)
ENST00000696260.1:n.2349-43_2349-42insTGGGTGTGTTT (FANCC)
ENST00000289081.8:c.1534-43_1534-42insTGGGTGTGTTT (FANCC) MANE Select	ENSP00000289081.3:n.1534-43_1534-42insTGGGTGTGTTT
ENST00000375305.6:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	ENSP00000364454.1:n.1534-43_1534-42insTGGGTGTGTTT
ENST00000649334.1:c.1679-43_1679-42insTGGGTGTGTTT (FANCC)	ENSP00000497735.1:n.1679-43_1679-42insTGGGTGTGTTT
ENST00000289081.7:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	ENSP00000289081.3:n.1534-43_1534-42insTGGGTGTGTTT
ENST00000375305.5:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	ENSP00000364454.1:n.1534-43_1534-42insTGGGTGTGTTT
NM_000136.2:c.1534-43_1534-42insTGGGTGTGTTT , LRG_497t1:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	NP_000127.2:n.1534-43_1534-42insTGGGTGTGTTT
NM_001243743.1:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	NP_001230672.1:n.1534-43_1534-42insTGGGTGTGTTT
XM_005251802.2:c.853-43_853-42insTGGGTGTGTTT (FANCC)	XP_005251859.1:n.853-43_853-42insTGGGTGTGTTT
XM_006717001.1:c.1369-43_1369-42insTGGGTGTGTTT (FANCC)	XP_006717064.1:n.1369-43_1369-42insTGGGTGTGTTT
XM_011518365.1:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	XP_011516667.1:n.1534-43_1534-42insTGGGTGTGTTT
XM_011518367.1:c.1078-43_1078-42insTGGGTGTGTTT (FANCC)	XP_011516669.1:n.1078-43_1078-42insTGGGTGTGTTT
XM_011519121.1:c.2319+21113_2319+21114insAACACACCCAA (AOPEP)	XP_011517423.1:n.2319+21113_2319+21114insAACACACCCAA
XM_005251802.3:c.853-43_853-42insTGGGTGTGTTT (FANCC)	XP_005251859.1:n.853-43_853-42insTGGGTGTGTTT
XM_006717001.3:c.1369-43_1369-42insTGGGTGTGTTT (FANCC)	XP_006717064.1:n.1369-43_1369-42insTGGGTGTGTTT
XM_011518365.3:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	XP_011516667.1:n.1534-43_1534-42insTGGGTGTGTTT
XM_011518367.2:c.1078-43_1078-42insTGGGTGTGTTT (FANCC)	XP_011516669.1:n.1078-43_1078-42insTGGGTGTGTTT
XM_011519121.3:c.2319+21113_2319+21114insAACACACCCAA (AOPEP)	XP_011517423.1:n.2319+21113_2319+21114insAACACACCCAA
XM_017014452.2:c.1078-43_1078-42insTGGGTGTGTTT (FANCC)	XP_016869941.1:n.1078-43_1078-42insTGGGTGTGTTT
XM_017014453.1:c.1078-43_1078-42insTGGGTGTGTTT (FANCC)	XP_016869942.1:n.1078-43_1078-42insTGGGTGTGTTT
XM_017014454.1:c.913-43_913-42insTGGGTGTGTTT (FANCC)	XP_016869943.1:n.913-43_913-42insTGGGTGTGTTT
XM_024447451.1:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	XP_024303219.1:n.1534-43_1534-42insTGGGTGTGTTT
NM_000136.3:c.1534-43_1534-42insTGGGTGTGTTT (FANCC) MANE Select	NP_000127.2:n.1534-43_1534-42insTGGGTGTGTTT
NM_001243743.2:c.1534-43_1534-42insTGGGTGTGTTT (FANCC)	NP_001230672.1:n.1534-43_1534-42insTGGGTGTGTTT