Canonical Allele Identifier: CA9091391
Community Standard Title: NM_032607.3(CREB3L3):c.577-2A>G
Gene: CREB3L3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4164501A>G , CM000681.2:g.4164501A>G GRCh38
NC_000019.9:g.4164498A>G , CM000681.1:g.4164498A>G GRCh37
NC_000019.8:g.4115498A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032607.3:c.577-2A>G MANE Select NP_115996.1:n.577-2A>G
ENST00000078445.7:c.577-2A>G MANE Select ENSP00000078445.1:n.577-2A>G
NM_001271995.1:c.574-2A>G NP_001258924.1:n.574-2A>G
NM_001271995.2:c.574-2A>G NP_001258924.1:n.574-2A>G
NM_001271996.1:c.577-8A>G NP_001258925.1:n.577-8A>G
NM_001271996.2:c.577-8A>G NP_001258925.1:n.577-8A>G
NM_001271997.1:c.577-2A>G NP_001258926.1:n.577-2A>G
NM_001271997.2:c.577-2A>G NP_001258926.1:n.577-2A>G
NM_032607.2:c.577-2A>G NP_115996.1:n.577-2A>G
ENST00000078445.6:c.577-2A>G ENSP00000078445.1:n.577-2A>G
ENST00000595923.5:c.574-2A>G ENSP00000469355.1:n.574-2A>G
ENST00000598894.1:n.59A>G
ENST00000602147.1:c.577-2A>G ENSP00000470119.1:n.577-2A>G
ENST00000602257.5:c.577-8A>G ENSP00000472399.1:n.577-8A>G