Canonical Allele Identifier: CA203390087

Gene: HSPA14 MSANTD7

Linked Data

• dbSNP Id: rs912527067
• MyVariant Identifiers: chr10:g.14888747G>A (hg19) ; chr10:g.14846748G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846748G>A , CM000672.2:g.14846748G>A	GRCh38
NC_000010.10:g.14888747G>A , CM000672.1:g.14888747G>A	GRCh37
NC_000010.9:g.14928753G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378372.8:c.222-1861G>A (HSPA14) MANE Select	ENSP00000367623.3:n.222-1861G>A
ENST00000640019.3:c.*2854G>A (MSANTD7) MANE Select	ENSP00000491568.1:n.*2854G>A
ENST00000378372.7:c.222-1861G>A (HSPA14)	ENSP00000367623.3:n.222-1861G>A
ENST00000441647.1:c.188-1861G>A (HSPA14)
NM_001278205.1:c.*3167G>A (HSPA14)	NP_001265134.1:n.*3167G>A
NM_016299.3:c.222-1861G>A (HSPA14)	NP_057383.2:n.222-1861G>A
NR_103464.1:n.4555G>A (HSPA14)
NM_016299.4:c.222-1861G>A (HSPA14) MANE Select	NP_057383.2:n.222-1861G>A
NR_103464.2:n.4409G>A (HSPA14)
NM_001378785.1:c.*2854G>A (MSANTD7) MANE Select	NP_001365714.1:n.*2854G>A
NM_001378790.1:c.*2854G>A (MSANTD7)	NP_001365719.1:n.*2854G>A