Canonical Allele Identifier: CA1892320442
Gene: HSPA14 HGNC NCBI
MSANTD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.14846911_14846912delinsTA , CM000672.2:g.14846911_14846912delinsTA GRCh38
NC_000010.10:g.14888910_14888911delinsTA , CM000672.1:g.14888910_14888911delinsTA GRCh37
NC_000010.9:g.14928916_14928917delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000378372.8:c.222-1698_222-1697delinsTA (HSPA14) MANE Select ENSP00000367623.3:n.222-1698_222-1697deli...
ENST00000640019.3:c.*3017_*3018delinsTA (MSANTD7) MANE Select ENSP00000491568.1:n.*3017_*3018delinsTA
ENST00000378372.7:c.222-1698_222-1697delinsTA (HSPA14) ENSP00000367623.3:n.222-1698_222-1697deli...
ENST00000441647.1:c.188-1698_188-1697delinsTA (HSPA14)
NM_001278205.1:c.*3330_*3331delinsTA (HSPA14) NP_001265134.1:n.*3330_*3331delinsTA
NM_016299.3:c.222-1698_222-1697delinsTA (HSPA14) NP_057383.2:n.222-1698_222-1697delinsTA
NR_103464.1:n.4718_4719delinsTA (HSPA14)
NM_016299.4:c.222-1698_222-1697delinsTA (HSPA14) MANE Select NP_057383.2:n.222-1698_222-1697delinsTA
NR_103464.2:n.4572_4573delinsTA (HSPA14)
NM_001378785.1:c.*3017_*3018delinsTA (MSANTD7) MANE Select NP_001365714.1:n.*3017_*3018delinsTA
NM_001378790.1:c.*3017_*3018delinsTA (MSANTD7) NP_001365719.1:n.*3017_*3018delinsTA