Canonical Allele Identifier: CA2657267289
Gene: UPK3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293380C>G , CM000684.2:g.45293380C>G GRCh38
NC_000022.10:g.45689261C>G , CM000684.1:g.45689261C>G GRCh37
NC_000022.9:g.44067925C>G NCBI36
NG_016203.1:g.13394C>G
NG_016203.2:g.13394C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+67C>G MANE Select ENSP00000216211.4:n.704+67C>G
ENST00000216211.8:c.704+67C>G ENSP00000216211.4:n.704+67C>G
ENST00000396082.2:c.341+67C>G ENSP00000379391.2:n.341+67C>G
NM_001167574.1:c.341+67C>G NP_001161046.1:n.341+67C>G
NM_006953.3:c.704+67C>G NP_008884.1:n.704+67C>G
XM_011530364.1:c.710+67C>G XP_011528666.1:n.710+67C>G
XM_011530365.1:c.347+67C>G XP_011528667.1:n.347+67C>G
NM_006953.4:c.704+67C>G MANE Select NP_008884.1:n.704+67C>G
NM_001167574.2:c.341+67C>G NP_001161046.1:n.341+67C>G