Canonical Allele Identifier: CA1892320452
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846938C= , CM000672.2:g.14846938C= GRCh38
NC_000010.10:g.14888937C= , CM000672.1:g.14888937C= GRCh37
NC_000010.9:g.14928943C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1671C= (HSPA14) MANE Select ENSP00000367623.3:n.222-1671C=
ENST00000640019.3:c.*3044C= (MSANTD7) MANE Select ENSP00000491568.1:n.*3044C=
ENST00000378372.7:c.222-1671C= (HSPA14) ENSP00000367623.3:n.222-1671C=
ENST00000441647.1:c.188-1671C= (HSPA14)
NM_001278205.1:c.*3357C= (HSPA14) NP_001265134.1:n.*3357C=
NM_016299.3:c.222-1671C= (HSPA14) NP_057383.2:n.222-1671C=
NR_103464.1:n.4745C= (HSPA14)
NM_016299.4:c.222-1671C= (HSPA14) MANE Select NP_057383.2:n.222-1671C=
NR_103464.2:n.4599C= (HSPA14)
NM_001378785.1:c.*3044C= (MSANTD7) MANE Select NP_001365714.1:n.*3044C=
NM_001378790.1:c.*3044C= (MSANTD7) NP_001365719.1:n.*3044C=