Canonical Allele Identifier: CA203390208
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Linked Data

dbSNP Id: rs769547693

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846913del , CM000672.2:g.14846913del GRCh38
NC_000010.10:g.14888912del , CM000672.1:g.14888912del GRCh37
NC_000010.9:g.14928918del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1696del (HSPA14) MANE Select ENSP00000367623.3:n.222-1696del
ENST00000640019.3:c.*3019del (MSANTD7) MANE Select ENSP00000491568.1:n.*3019del
ENST00000378372.7:c.222-1696del (HSPA14) ENSP00000367623.3:n.222-1696del
ENST00000441647.1:c.188-1696del (HSPA14)
NM_001278205.1:c.*3332del (HSPA14) NP_001265134.1:n.*3332del
NM_016299.3:c.222-1696del (HSPA14) NP_057383.2:n.222-1696del
NR_103464.1:n.4720del (HSPA14)
NM_016299.4:c.222-1696del (HSPA14) MANE Select NP_057383.2:n.222-1696del
NR_103464.2:n.4574del (HSPA14)
NM_001378785.1:c.*3019del (MSANTD7) MANE Select NP_001365714.1:n.*3019del
NM_001378790.1:c.*3019del (MSANTD7) NP_001365719.1:n.*3019del