Canonical Allele Identifier: CA662145689

Gene: HSPA14 MSANTD7

Linked Data

• dbSNP Id: rs1235454348
• gnomAD v3: 10-14846915-G-T
• gnomAD v4: 10-14846915-G-T
• MyVariant Identifiers: chr10:g.14888914G>T (hg19) ; chr10:g.14846915G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846915G>T , CM000672.2:g.14846915G>T	GRCh38
NC_000010.10:g.14888914G>T , CM000672.1:g.14888914G>T	GRCh37
NC_000010.9:g.14928920G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1694G>T (HSPA14) MANE Select	ENSP00000367623.3:n.222-1694G>T
ENST00000640019.3:c.*3021G>T (MSANTD7) MANE Select	ENSP00000491568.1:n.*3021G>T
ENST00000378372.7:c.222-1694G>T (HSPA14)	ENSP00000367623.3:n.222-1694G>T
ENST00000441647.1:c.188-1694G>T (HSPA14)
NM_001278205.1:c.*3334G>T (HSPA14)	NP_001265134.1:n.*3334G>T
NM_016299.3:c.222-1694G>T (HSPA14)	NP_057383.2:n.222-1694G>T
NR_103464.1:n.4722G>T (HSPA14)
NM_016299.4:c.222-1694G>T (HSPA14) MANE Select	NP_057383.2:n.222-1694G>T
NR_103464.2:n.4576G>T (HSPA14)
NM_001378785.1:c.*3021G>T (MSANTD7) MANE Select	NP_001365714.1:n.*3021G>T
NM_001378790.1:c.*3021G>T (MSANTD7)	NP_001365719.1:n.*3021G>T