Canonical Allele Identifier: CA2408185541

Gene: UPK3A

Linked Data

• dbSNP Id: rs2084175880

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45293470_45293473dup , CM000684.2:g.45293470_45293473dup	GRCh38
NC_000022.10:g.45689351_45689354dup , CM000684.1:g.45689351_45689354dup	GRCh37
NC_000022.9:g.44068015_44068018dup	NCBI36
NG_016203.1:g.13484_13487dup
NG_016203.2:g.13484_13487dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216211.9:c.704+157_704+160dup MANE Select	ENSP00000216211.4:n.704+157_704+160dup
ENST00000216211.8:c.704+157_704+160dup	ENSP00000216211.4:n.704+157_704+160dup
ENST00000396082.2:c.341+157_341+160dup	ENSP00000379391.2:n.341+157_341+160dup
NM_001167574.1:c.341+157_341+160dup	NP_001161046.1:n.341+157_341+160dup
NM_006953.3:c.704+157_704+160dup	NP_008884.1:n.704+157_704+160dup
XM_011530364.1:c.710+157_710+160dup	XP_011528666.1:n.710+157_710+160dup
XM_011530365.1:c.347+157_347+160dup	XP_011528667.1:n.347+157_347+160dup
NM_006953.4:c.704+157_704+160dup MANE Select	NP_008884.1:n.704+157_704+160dup
NM_001167574.2:c.341+157_341+160dup	NP_001161046.1:n.341+157_341+160dup