Canonical Allele Identifier: CA592105578

Gene: HSPA14 MSANTD7

Linked Data

• dbSNP Id: rs915288353
• gnomAD v2: 10-14888929-A-T
• gnomAD v3: 10-14846930-A-T
• gnomAD v4: 10-14846930-A-T
• MyVariant Identifiers: chr10:g.14888929A>T (hg19) ; chr10:g.14846930A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846930A>T , CM000672.2:g.14846930A>T	GRCh38
NC_000010.10:g.14888929A>T , CM000672.1:g.14888929A>T	GRCh37
NC_000010.9:g.14928935A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1679A>T (HSPA14) MANE Select	ENSP00000367623.3:n.222-1679A>T
ENST00000640019.3:c.*3036A>T (MSANTD7) MANE Select	ENSP00000491568.1:n.*3036A>T
ENST00000378372.7:c.222-1679A>T (HSPA14)	ENSP00000367623.3:n.222-1679A>T
ENST00000441647.1:c.188-1679A>T (HSPA14)
NM_001278205.1:c.*3349A>T (HSPA14)	NP_001265134.1:n.*3349A>T
NM_016299.3:c.222-1679A>T (HSPA14)	NP_057383.2:n.222-1679A>T
NR_103464.1:n.4737A>T (HSPA14)
NM_016299.4:c.222-1679A>T (HSPA14) MANE Select	NP_057383.2:n.222-1679A>T
NR_103464.2:n.4591A>T (HSPA14)
NM_001378785.1:c.*3036A>T (MSANTD7) MANE Select	NP_001365714.1:n.*3036A>T
NM_001378790.1:c.*3036A>T (MSANTD7)	NP_001365719.1:n.*3036A>T