Canonical Allele Identifier: CA2608345637
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Linked Data

gnomAD v4: 10-14846734-T-A
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Genomic Alleles

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

Transcript Alleles

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