Canonical Allele Identifier: CA2608345638

Gene: HSPA14 MSANTD7

Linked Data

• gnomAD v4: 10-14846734-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846734T>C , CM000672.2:g.14846734T>C	GRCh38
NC_000010.10:g.14888733T>C , CM000672.1:g.14888733T>C	GRCh37
NC_000010.9:g.14928739T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1875T>C (HSPA14) MANE Select	ENSP00000367623.3:n.222-1875T>C
ENST00000640019.3:c.*2840T>C (MSANTD7) MANE Select	ENSP00000491568.1:n.*2840T>C
ENST00000378372.7:c.222-1875T>C (HSPA14)	ENSP00000367623.3:n.222-1875T>C
ENST00000441647.1:c.188-1875T>C (HSPA14)
NM_001278205.1:c.*3153T>C (HSPA14)	NP_001265134.1:n.*3153T>C
NM_016299.3:c.222-1875T>C (HSPA14)	NP_057383.2:n.222-1875T>C
NR_103464.1:n.4541T>C (HSPA14)
NM_016299.4:c.222-1875T>C (HSPA14) MANE Select	NP_057383.2:n.222-1875T>C
NR_103464.2:n.4395T>C (HSPA14)
NM_001378785.1:c.*2840T>C (MSANTD7) MANE Select	NP_001365714.1:n.*2840T>C
NM_001378790.1:c.*2840T>C (MSANTD7)	NP_001365719.1:n.*2840T>C