Canonical Allele Identifier: CA1224739908
Gene: H3-3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226064465A= , CM000663.2:g.226064465A= GRCh38
NC_000001.10:g.226252166A= , CM000663.1:g.226252166A= GRCh37
NC_000001.9:g.224318789A= NCBI36
NG_065173.1:g.6759A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366815.10:c.114A= MANE Select ENSP00000355780.3:p.Lys38=
ENST00000653960.1:n.223A=
ENST00000655399.1:c.114A= ENSP00000499800.1:p.Lys38=
ENST00000656829.1:n.30-1270A=
ENST00000661429.1:c.114A= ENSP00000499385.1:p.Lys38=
ENST00000666609.1:c.114A= ENSP00000499275.1:p.Lys38=
ENST00000667897.1:c.114A= ENSP00000499446.1:p.Lys38=
ENST00000366813.1:c.114A= ENSP00000355778.1:p.Lys38=
ENST00000366814.3:c.114A= ENSP00000355779.3:p.Lys38=
ENST00000366815.7:c.114A= ENSP00000355780.3:p.Lys38=
ENST00000366816.5:c.114A= ENSP00000355781.1:p.Lys38=
NM_002107.4:c.114A= NP_002098.1:p.Lys38=
NM_002107.5:c.114A= NP_002098.1:p.Lys38=
NM_002107.7:c.114A= MANE Select NP_002098.1:p.Lys38=
NM_001379043.1:c.114A= NP_001365972.1:p.Lys38=
NM_001379045.1:c.114A= NP_001365974.1:p.Lys38=
NM_001379046.1:c.114A= NP_001365975.1:p.Lys38=
NM_001379047.1:c.114A= NP_001365976.1:p.Lys38=