Canonical Allele Identifier: CA2793937037

Gene: HSPA8 SNORD14D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058983_123058984insAACACAC , CM000673.2:g.123058983_123058984insAACACAC	GRCh38
NC_000011.9:g.122929691_122929692insAACACAC , CM000673.1:g.122929691_122929692insAACACAC	GRCh37
NC_000011.8:g.122434901_122434902insAACACAC	NCBI36
NG_029473.1:g.8153_8154insGTGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+75_1323+76insGTGTGTT (HSPA8) MANE Select	ENSP00000432083.1:n.1323+75_1323+76insGTGTGTT
ENST00000227378.7:c.1323+75_1323+76insGTGTGTT (HSPA8)	ENSP00000227378.3:n.1323+75_1323+76insGTGTGTT
ENST00000453788.6:c.1323+75_1323+76insGTGTGTT (HSPA8)	ENSP00000404372.2:n.1323+75_1323+76insGTGTGTT
ENST00000524552.5:c.96+75_96+76insGTGTGTT (HSPA8)	ENSP00000435908.1:n.96+75_96+76insGTGTGTT
ENST00000526110.5:c.1266+75_1266+76insGTGTGTT (HSPA8)	ENSP00000433584.1:n.1266+75_1266+76insGTGTGTT
ENST00000526686.1:c.-175_-174insGTGTGTT (HSPA8)	ENSP00000435019.1:n.-175_-174insGTGTGTT
ENST00000532091.1:n.1145_1146insGTGTGTT (HSPA8)
ENST00000532636.5:c.1323+75_1323+76insGTGTGTT (HSPA8)	ENSP00000437125.1:n.1323+75_1323+76insGTGTGTT
ENST00000533238.5:n.425+75_425+76insGTGTGTT (HSPA8)
ENST00000533540.5:c.885+75_885+76insGTGTGTT (HSPA8)	ENSP00000437189.1:n.885+75_885+76insGTGTGTT
ENST00000534319.5:c.615+75_615+76insGTGTGTT (HSPA8)	ENSP00000433316.1:n.615+75_615+76insGTGTGTT
ENST00000534624.5:c.1323+75_1323+76insGTGTGTT (HSPA8)	ENSP00000432083.1:n.1323+75_1323+76insGTGTGTT
NM_006597.5:c.1323+75_1323+76insGTGTGTT (HSPA8)	NP_006588.1:n.1323+75_1323+76insGTGTGTT
NM_153201.3:c.1323+75_1323+76insGTGTGTT (HSPA8)	NP_694881.1:n.1323+75_1323+76insGTGTGTT
NR_001454.2:n.12_13insGTGTGTT (SNORD14D)
XM_011542798.1:c.1323+75_1323+76insGTGTGTT (HSPA8)	XP_011541100.1:n.1323+75_1323+76insGTGTGTT
NM_006597.6:c.1323+75_1323+76insGTGTGTT (HSPA8) MANE Select	NP_006588.1:n.1323+75_1323+76insGTGTGTT
NM_153201.4:c.1323+75_1323+76insGTGTGTT (HSPA8)	NP_694881.1:n.1323+75_1323+76insGTGTGTT