Canonical Allele Identifier: CA2616532843

Gene: HSPA8 SNORD14D

Linked Data

• gnomAD v4: 11-123058942-ATAAGACTTTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058944_123058953del , CM000673.2:g.123058944_123058953del	GRCh38
NC_000011.9:g.122929652_122929661del , CM000673.1:g.122929652_122929661del	GRCh37
NC_000011.8:g.122434862_122434871del	NCBI36
NG_029473.1:g.8185_8194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1323+107_1324-113del (HSPA8) MANE Select	ENSP00000432083.1:n.1323+107_1324-113del
ENST00000227378.7:c.1323+107_1324-113del (HSPA8)	ENSP00000227378.3:n.1323+107_1324-113del
ENST00000453788.6:c.1323+107_1324-113del (HSPA8)	ENSP00000404372.2:n.1323+107_1324-113del
ENST00000524552.5:c.96+107_97-113del (HSPA8)	ENSP00000435908.1:n.96+107_97-113del
ENST00000526110.5:c.1266+107_1267-113del (HSPA8)	ENSP00000433584.1:n.1266+107_1267-113del
ENST00000526686.1:c.-143_-134del (HSPA8)	ENSP00000435019.1:n.-143_-134del
ENST00000532091.1:n.1177_1186del (HSPA8)
ENST00000532636.5:c.1323+107_1324-113del (HSPA8)	ENSP00000437125.1:n.1323+107_1324-113del
ENST00000533238.5:n.425+107_426-113del (HSPA8)
ENST00000533540.5:c.885+107_886-113del (HSPA8)	ENSP00000437189.1:n.885+107_886-113del
ENST00000534319.5:c.615+107_616-113del (HSPA8)	ENSP00000433316.1:n.615+107_616-113del
ENST00000534624.5:c.1323+107_1324-113del (HSPA8)	ENSP00000432083.1:n.1323+107_1324-113del
NM_006597.5:c.1323+107_1324-113del (HSPA8)	NP_006588.1:n.1323+107_1324-113del
NM_153201.3:c.1323+107_1324-113del (HSPA8)	NP_694881.1:n.1323+107_1324-113del
NR_001454.2:n.44_53del (SNORD14D)
XM_011542798.1:c.1323+107_1324-113del (HSPA8)	XP_011541100.1:n.1323+107_1324-113del
NM_006597.6:c.1323+107_1324-113del (HSPA8) MANE Select	NP_006588.1:n.1323+107_1324-113del
NM_153201.4:c.1323+107_1324-113del (HSPA8)	NP_694881.1:n.1323+107_1324-113del