Canonical Allele Identifier: CA1913178417
Gene: BICC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.58811675C>G , CM000672.2:g.58811675C>G GRCh38
NC_000010.10:g.60571435C>G , CM000672.1:g.60571435C>G GRCh37
NC_000010.9:g.60241441C>G NCBI36
NG_029759.2:g.303532C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373886.8:c.2377-2155C>G MANE Select ENSP00000362993.3:n.2377-2155C>G
ENST00000263103.1:c.1255-2155C>G ENSP00000263103.1:n.1255-2155C>G
ENST00000373886.7:c.2377-2155C>G ENSP00000362993.3:n.2377-2155C>G
NM_001080512.2:c.2377-2155C>G NP_001073981.1:n.2377-2155C>G
XM_005270169.3:c.2236-2155C>G XP_005270226.1:n.2236-2155C>G
XM_011540185.1:c.2449-2155C>G XP_011538487.1:n.2449-2155C>G
XM_011540186.1:c.2446-2155C>G XP_011538488.1:n.2446-2155C>G
XM_011540187.1:c.2449-2155C>G XP_011538489.1:n.2449-2155C>G
XM_011540188.1:c.2233-2155C>G XP_011538490.1:n.2233-2155C>G
XM_011540189.1:c.2221-2155C>G XP_011538491.1:n.2221-2155C>G
XM_011540190.1:c.2137-2155C>G XP_011538492.1:n.2137-2155C>G
XM_011540191.1:c.1993-2155C>G XP_011538493.1:n.1993-2155C>G
XM_005270169.5:c.2236-2155C>G XP_005270226.1:n.2236-2155C>G
XM_011540185.2:c.2449-2155C>G XP_011538487.1:n.2449-2155C>G
XM_011540190.3:c.2137-2155C>G XP_011538492.1:n.2137-2155C>G
XM_011540191.2:c.1993-2155C>G XP_011538493.1:n.1993-2155C>G
XM_017016677.1:c.2245-2155C>G XP_016872166.1:n.2245-2155C>G
XM_017016678.1:c.2233-2155C>G XP_016872167.1:n.2233-2155C>G
XM_024448174.1:c.2464-2155C>G XP_024303942.1:n.2464-2155C>G
XM_024448175.1:c.2137-2155C>G XP_024303943.1:n.2137-2155C>G
NM_001080512.3:c.2377-2155C>G MANE Select NP_001073981.1:n.2377-2155C>G