Canonical Allele Identifier: CA943027893
Gene: HSPA8 HGNC NCBI
SNORD14D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058943_123058944insTAGCC , CM000673.2:g.123058943_123058944insTAGCC GRCh38
NC_000011.9:g.122929651_122929652insTAGCC , CM000673.1:g.122929651_122929652insTAGCC GRCh37
NC_000011.8:g.122434861_122434862insTAGCC NCBI36
NG_029473.1:g.8193_8194insGGCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1324-114_1324-113insGGCTA (HSPA8) MANE Select ENSP00000432083.1:n.1324-114_1324-113insGGCTA
ENST00000227378.7:c.1324-114_1324-113insGGCTA (HSPA8) ENSP00000227378.3:n.1324-114_1324-113insGGCTA
ENST00000453788.6:c.1324-114_1324-113insGGCTA (HSPA8) ENSP00000404372.2:n.1324-114_1324-113insGGCTA
ENST00000524552.5:c.97-114_97-113insGGCTA (HSPA8) ENSP00000435908.1:n.97-114_97-113insGGCTA
ENST00000526110.5:c.1267-114_1267-113insGGCTA (HSPA8) ENSP00000433584.1:n.1267-114_1267-113insGGCTA
ENST00000526686.1:c.-135_-134insGGCTA (HSPA8) ENSP00000435019.1:n.-135_-134insGGCTA
ENST00000532091.1:n.1185_1186insGGCTA (HSPA8)
ENST00000532636.5:c.1324-114_1324-113insGGCTA (HSPA8) ENSP00000437125.1:n.1324-114_1324-113insGGCTA
ENST00000533238.5:n.426-114_426-113insGGCTA (HSPA8)
ENST00000533540.5:c.886-114_886-113insGGCTA (HSPA8) ENSP00000437189.1:n.886-114_886-113insGGCTA
ENST00000534319.5:c.616-114_616-113insGGCTA (HSPA8) ENSP00000433316.1:n.616-114_616-113insGGCTA
ENST00000534624.5:c.1324-114_1324-113insGGCTA (HSPA8) ENSP00000432083.1:n.1324-114_1324-113insGGCTA
NM_006597.5:c.1324-114_1324-113insGGCTA (HSPA8) NP_006588.1:n.1324-114_1324-113insGGCTA
NM_153201.3:c.1324-114_1324-113insGGCTA (HSPA8) NP_694881.1:n.1324-114_1324-113insGGCTA
NR_001454.2:n.52_53insGGCTA (SNORD14D)
XM_011542798.1:c.1324-114_1324-113insGGCTA (HSPA8) XP_011541100.1:n.1324-114_1324-113insGGCTA
NM_006597.6:c.1324-114_1324-113insGGCTA (HSPA8) MANE Select NP_006588.1:n.1324-114_1324-113insGGCTA
NM_153201.4:c.1324-114_1324-113insGGCTA (HSPA8) NP_694881.1:n.1324-114_1324-113insGGCTA