Canonical Allele Identifier: CA2575011593

Gene: HSPA8 SNORD14D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058982del , CM000673.2:g.123058982del	GRCh38
NC_000011.9:g.122929690del , CM000673.1:g.122929690del	GRCh37
NC_000011.8:g.122434900del	NCBI36
NG_029473.1:g.8156del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+78del (HSPA8) MANE Select	ENSP00000432083.1:n.1323+78del
ENST00000227378.7:c.1323+78del (HSPA8)	ENSP00000227378.3:n.1323+78del
ENST00000453788.6:c.1323+78del (HSPA8)	ENSP00000404372.2:n.1323+78del
ENST00000524552.5:c.96+78del (HSPA8)	ENSP00000435908.1:n.96+78del
ENST00000526110.5:c.1266+78del (HSPA8)	ENSP00000433584.1:n.1266+78del
ENST00000526686.1:c.-172del (HSPA8)	ENSP00000435019.1:n.-172del
ENST00000532091.1:n.1148del (HSPA8)
ENST00000532636.5:c.1323+78del (HSPA8)	ENSP00000437125.1:n.1323+78del
ENST00000533238.5:n.425+78del (HSPA8)
ENST00000533540.5:c.885+78del (HSPA8)	ENSP00000437189.1:n.885+78del
ENST00000534319.5:c.615+78del (HSPA8)	ENSP00000433316.1:n.615+78del
ENST00000534624.5:c.1323+78del (HSPA8)	ENSP00000432083.1:n.1323+78del
NM_006597.5:c.1323+78del (HSPA8)	NP_006588.1:n.1323+78del
NM_153201.3:c.1323+78del (HSPA8)	NP_694881.1:n.1323+78del
NR_001454.2:n.15del (SNORD14D)
XM_011542798.1:c.1323+78del (HSPA8)	XP_011541100.1:n.1323+78del
NM_006597.6:c.1323+78del (HSPA8) MANE Select	NP_006588.1:n.1323+78del
NM_153201.4:c.1323+78del (HSPA8)	NP_694881.1:n.1323+78del