Canonical Allele Identifier: CA1892320367

Gene: HSPA14 MSANTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846742C= , CM000672.2:g.14846742C=	GRCh38
NC_000010.10:g.14888741C= , CM000672.1:g.14888741C=	GRCh37
NC_000010.9:g.14928747C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378372.8:c.222-1867C= (HSPA14) MANE Select	ENSP00000367623.3:n.222-1867C=
ENST00000640019.3:c.*2848C= (MSANTD7) MANE Select	ENSP00000491568.1:n.*2848C=
ENST00000378372.7:c.222-1867C= (HSPA14)	ENSP00000367623.3:n.222-1867C=
ENST00000441647.1:c.188-1867C= (HSPA14)
NM_001278205.1:c.*3161C= (HSPA14)	NP_001265134.1:n.*3161C=
NM_016299.3:c.222-1867C= (HSPA14)	NP_057383.2:n.222-1867C=
NR_103464.1:n.4549C= (HSPA14)
NM_016299.4:c.222-1867C= (HSPA14) MANE Select	NP_057383.2:n.222-1867C=
NR_103464.2:n.4403C= (HSPA14)
NM_001378785.1:c.*2848C= (MSANTD7) MANE Select	NP_001365714.1:n.*2848C=
NM_001378790.1:c.*2848C= (MSANTD7)	NP_001365719.1:n.*2848C=