Canonical Allele Identifier: CA1892320364

Gene: HSPA14 MSANTD7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.14846737_14846738delinsTG , CM000672.2:g.14846737_14846738delinsTG	GRCh38
NC_000010.10:g.14888736_14888737delinsTG , CM000672.1:g.14888736_14888737delinsTG	GRCh37
NC_000010.9:g.14928742_14928743delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000378372.8:c.222-1872_222-1871delinsTG (HSPA14) MANE Select	ENSP00000367623.3:n.222-1872_222-1871delinsTG
ENST00000640019.3:c.*2843_*2844delinsTG (MSANTD7) MANE Select	ENSP00000491568.1:n.*2843_*2844delinsTG
ENST00000378372.7:c.222-1872_222-1871delinsTG (HSPA14)	ENSP00000367623.3:n.222-1872_222-1871delinsTG
ENST00000441647.1:c.188-1872_188-1871delinsTG (HSPA14)
NM_001278205.1:c.*3156_*3157delinsTG (HSPA14)	NP_001265134.1:n.*3156_*3157delinsTG
NM_016299.3:c.222-1872_222-1871delinsTG (HSPA14)	NP_057383.2:n.222-1872_222-1871delinsTG
NR_103464.1:n.4544_4545delinsTG (HSPA14)
NM_016299.4:c.222-1872_222-1871delinsTG (HSPA14) MANE Select	NP_057383.2:n.222-1872_222-1871delinsTG
NR_103464.2:n.4398_4399delinsTG (HSPA14)
NM_001378785.1:c.*2843_*2844delinsTG (MSANTD7) MANE Select	NP_001365714.1:n.*2843_*2844delinsTG
NM_001378790.1:c.*2843_*2844delinsTG (MSANTD7)	NP_001365719.1:n.*2843_*2844delinsTG