Canonical Allele Identifier: CA203390206
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Linked Data

dbSNP Id: rs12770170

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846907T>C , CM000672.2:g.14846907T>C GRCh38
NC_000010.10:g.14888906T>C , CM000672.1:g.14888906T>C GRCh37
NC_000010.9:g.14928912T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1702T>C (HSPA14) MANE Select ENSP00000367623.3:n.222-1702T>C
ENST00000640019.3:c.*3013T>C (MSANTD7) MANE Select ENSP00000491568.1:n.*3013T>C
ENST00000378372.7:c.222-1702T>C (HSPA14) ENSP00000367623.3:n.222-1702T>C
ENST00000441647.1:c.188-1702T>C (HSPA14)
NM_001278205.1:c.*3326T>C (HSPA14) NP_001265134.1:n.*3326T>C
NM_016299.3:c.222-1702T>C (HSPA14) NP_057383.2:n.222-1702T>C
NR_103464.1:n.4714T>C (HSPA14)
NM_016299.4:c.222-1702T>C (HSPA14) MANE Select NP_057383.2:n.222-1702T>C
NR_103464.2:n.4568T>C (HSPA14)
NM_001378785.1:c.*3013T>C (MSANTD7) MANE Select NP_001365714.1:n.*3013T>C
NM_001378790.1:c.*3013T>C (MSANTD7) NP_001365719.1:n.*3013T>C