Canonical Allele Identifier: CA2454589949
Gene: UBE2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.119583024C= , CM000685.2:g.119583024C= GRCh38
NC_000023.10:g.118716987C= , CM000685.1:g.118716987C= GRCh37
NC_000023.9:g.118601015C= NCBI36
NG_009267.1:g.13489C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696533.1:c.547-103C= ENSP00000512694.1:n.547-103C=
ENST00000696534.1:c.331-103C= ENSP00000512695.1:n.331-103C=
ENST00000696539.1:c.547-103C= ENSP00000512700.1:n.547-103C=
ENST00000371558.7:c.331-103C= MANE Select ENSP00000360613.2:n.331-103C=
ENST00000346330.6:c.322-103C= ENSP00000335027.4:n.322-103C=
ENST00000371558.6:c.331-103C= ENSP00000360613.2:n.331-103C=
ENST00000371569.6:n.1352-103C=
ENST00000625938.2:c.241-103C= ENSP00000486599.1:n.241-103C=
ENST00000628549.1:c.232-103C= ENSP00000487203.1:n.232-103C=
ENST00000628734.1:n.310-103C=
ENST00000630695.2:c.106-103C= ENSP00000486550.1:n.106-103C=
ENST00000631185.2:c.330+348C= ENSP00000486153.1:n.330+348C=
NM_001282161.1:c.232-103C= NP_001269090.1:n.232-103C=
NM_003336.3:c.331-103C= NP_003327.2:n.331-103C=
NM_181762.2:c.241-103C= NP_861427.1:n.241-103C=
NM_003336.4:c.331-103C= MANE Select NP_003327.2:n.331-103C=
NM_001282161.2:c.232-103C= NP_001269090.1:n.232-103C=
NM_181762.3:c.241-103C= NP_861427.1:n.241-103C=