Canonical Allele Identifier: CA2587878773
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714552_6714553insAGACACT , CM000681.2:g.6714552_6714553insAGACACT GRCh38
NC_000019.9:g.6714563_6714564insAGACACT , CM000681.1:g.6714563_6714564insAGACACT GRCh37
NC_000019.8:g.6665563_6665564insAGACACT NCBI36
NG_009557.1:g.11100_11101insGTGTCTA , LRG_27:g.11100_11101insGTGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-106_382-105insGTGTCTA ENSP00000512083.1:n.382-106_382-105insGTGTCTA
ENST00000245907.11:c.505-106_505-105insGTGTCTA MANE Select ENSP00000245907.4:n.505-106_505-105insGTGTCTA
ENST00000245907.10:c.505-106_505-105insGTGTCTA ENSP00000245907.4:n.505-106_505-105insGTGTCTA
NM_000064.3:c.505-106_505-105insGTGTCTA NP_000055.2:n.505-106_505-105insGTGTCTA
NM_000064.4:c.505-106_505-105insGTGTCTA MANE Select NP_000055.2:n.505-106_505-105insGTGTCTA