Canonical Allele Identifier: CA203390221

Gene: HSPA14 MSANTD7

Linked Data

• dbSNP Id: rs1003987162
• gnomAD v2: 10-14888917-C-G
• gnomAD v3: 10-14846918-C-G
• gnomAD v4: 10-14846918-C-G
• MyVariant Identifiers: chr10:g.14888917C>G (hg19) ; chr10:g.14846918C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846918C>G , CM000672.2:g.14846918C>G	GRCh38
NC_000010.10:g.14888917C>G , CM000672.1:g.14888917C>G	GRCh37
NC_000010.9:g.14928923C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1691C>G (HSPA14) MANE Select	ENSP00000367623.3:n.222-1691C>G
ENST00000640019.3:c.*3024C>G (MSANTD7) MANE Select	ENSP00000491568.1:n.*3024C>G
ENST00000378372.7:c.222-1691C>G (HSPA14)	ENSP00000367623.3:n.222-1691C>G
ENST00000441647.1:c.188-1691C>G (HSPA14)
NM_001278205.1:c.*3337C>G (HSPA14)	NP_001265134.1:n.*3337C>G
NM_016299.3:c.222-1691C>G (HSPA14)	NP_057383.2:n.222-1691C>G
NR_103464.1:n.4725C>G (HSPA14)
NM_016299.4:c.222-1691C>G (HSPA14) MANE Select	NP_057383.2:n.222-1691C>G
NR_103464.2:n.4579C>G (HSPA14)
NM_001378785.1:c.*3024C>G (MSANTD7) MANE Select	NP_001365714.1:n.*3024C>G
NM_001378790.1:c.*3024C>G (MSANTD7)	NP_001365719.1:n.*3024C>G