Canonical Allele Identifier: CA2608345683
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846810_14846821dup , CM000672.2:g.14846810_14846821dup GRCh38
NC_000010.10:g.14888809_14888820dup , CM000672.1:g.14888809_14888820dup GRCh37
NC_000010.9:g.14928815_14928826dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1799_222-1788dup (HSPA14) MANE Select ENSP00000367623.3:n.222-1799_222-1788dup
ENST00000640019.3:c.*2916_*2927dup (MSANTD7) MANE Select ENSP00000491568.1:n.*2916_*2927dup
ENST00000378372.7:c.222-1799_222-1788dup (HSPA14) ENSP00000367623.3:n.222-1799_222-1788dup
ENST00000441647.1:c.188-1799_188-1788dup (HSPA14)
NM_001278205.1:c.*3229_*3240dup (HSPA14) NP_001265134.1:n.*3229_*3240dup
NM_016299.3:c.222-1799_222-1788dup (HSPA14) NP_057383.2:n.222-1799_222-1788dup
NR_103464.1:n.4617_4628dup (HSPA14)
NM_016299.4:c.222-1799_222-1788dup (HSPA14) MANE Select NP_057383.2:n.222-1799_222-1788dup
NR_103464.2:n.4471_4482dup (HSPA14)
NM_001378785.1:c.*2916_*2927dup (MSANTD7) MANE Select NP_001365714.1:n.*2916_*2927dup
NM_001378790.1:c.*2916_*2927dup (MSANTD7) NP_001365719.1:n.*2916_*2927dup