Canonical Allele Identifier: CA2608345635

Gene: HSPA14 MSANTD7

Linked Data

• gnomAD v4: 10-14846731-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846731C>T , CM000672.2:g.14846731C>T	GRCh38
NC_000010.10:g.14888730C>T , CM000672.1:g.14888730C>T	GRCh37
NC_000010.9:g.14928736C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1878C>T (HSPA14) MANE Select	ENSP00000367623.3:n.222-1878C>T
ENST00000640019.3:c.*2837C>T (MSANTD7) MANE Select	ENSP00000491568.1:n.*2837C>T
ENST00000378372.7:c.222-1878C>T (HSPA14)	ENSP00000367623.3:n.222-1878C>T
ENST00000441647.1:c.188-1878C>T (HSPA14)
NM_001278205.1:c.*3150C>T (HSPA14)	NP_001265134.1:n.*3150C>T
NM_016299.3:c.222-1878C>T (HSPA14)	NP_057383.2:n.222-1878C>T
NR_103464.1:n.4538C>T (HSPA14)
NM_016299.4:c.222-1878C>T (HSPA14) MANE Select	NP_057383.2:n.222-1878C>T
NR_103464.2:n.4392C>T (HSPA14)
NM_001378785.1:c.*2837C>T (MSANTD7) MANE Select	NP_001365714.1:n.*2837C>T
NM_001378790.1:c.*2837C>T (MSANTD7)	NP_001365719.1:n.*2837C>T