Canonical Allele Identifier: CA925197871
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Linked Data

dbSNP Id: rs1834061200
gnomAD v3: 10-14846826-G-C
gnomAD v4: 10-14846826-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846826G>C , CM000672.2:g.14846826G>C GRCh38
NC_000010.10:g.14888825G>C , CM000672.1:g.14888825G>C GRCh37
NC_000010.9:g.14928831G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1783G>C (HSPA14) MANE Select ENSP00000367623.3:n.222-1783G>C
ENST00000640019.3:c.*2932G>C (MSANTD7) MANE Select ENSP00000491568.1:n.*2932G>C
ENST00000378372.7:c.222-1783G>C (HSPA14) ENSP00000367623.3:n.222-1783G>C
ENST00000441647.1:c.188-1783G>C (HSPA14)
NM_001278205.1:c.*3245G>C (HSPA14) NP_001265134.1:n.*3245G>C
NM_016299.3:c.222-1783G>C (HSPA14) NP_057383.2:n.222-1783G>C
NR_103464.1:n.4633G>C (HSPA14)
NM_016299.4:c.222-1783G>C (HSPA14) MANE Select NP_057383.2:n.222-1783G>C
NR_103464.2:n.4487G>C (HSPA14)
NM_001378785.1:c.*2932G>C (MSANTD7) MANE Select NP_001365714.1:n.*2932G>C
NM_001378790.1:c.*2932G>C (MSANTD7) NP_001365719.1:n.*2932G>C
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Search 100 bp 3'