Canonical Allele Identifier: CA602581134

Gene: HSPA8 SNORD14C

Linked Data

• dbSNP Id: rs1358792897
• gnomAD v2: 11-122930056-CAAGG-C
• gnomAD v4: 11-123059348-CAAGG-C
• MyVariant Identifiers: chr11:g.122930057_122930060del (hg19) ; chr11:g.123059349_123059352del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059353_123059356del , CM000673.2:g.123059353_123059356del	GRCh38
NC_000011.9:g.122930061_122930064del , CM000673.1:g.122930061_122930064del	GRCh37
NC_000011.8:g.122435271_122435274del	NCBI36
NG_029473.1:g.7785_7788del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-91_1121-88del (HSPA8) MANE Select	ENSP00000432083.1:n.1121-91_1121-88del
ENST00000227378.7:c.1121-91_1121-88del (HSPA8)	ENSP00000227378.3:n.1121-91_1121-88del
ENST00000453788.6:c.1121-91_1121-88del (HSPA8)	ENSP00000404372.2:n.1121-91_1121-88del
ENST00000524552.5:c.-198_-195del (HSPA8)	ENSP00000435908.1:n.-198_-195del
ENST00000526110.5:c.1064-91_1064-88del (HSPA8)	ENSP00000433584.1:n.1064-91_1064-88del
ENST00000526862.1:n.399-91_399-88del (HSPA8)
ENST00000527983.5:n.1390_1393del (HSPA8)
ENST00000532091.1:n.868-91_868-88del (HSPA8)
ENST00000532636.5:c.1121-91_1121-88del (HSPA8)	ENSP00000437125.1:n.1121-91_1121-88del
ENST00000533238.5:n.381-249_381-246del (HSPA8)
ENST00000533540.5:c.683-91_683-88del (HSPA8)	ENSP00000437189.1:n.683-91_683-88del
ENST00000534319.5:c.413-91_413-88del (HSPA8)	ENSP00000433316.1:n.413-91_413-88del
ENST00000534624.5:c.1121-91_1121-88del (HSPA8)	ENSP00000432083.1:n.1121-91_1121-88del
NM_006597.5:c.1121-91_1121-88del (HSPA8)	NP_006588.1:n.1121-91_1121-88del
NM_153201.3:c.1121-91_1121-88del (HSPA8)	NP_694881.1:n.1121-91_1121-88del
NR_001453.2:n.71_74del (SNORD14C)
XM_011542798.1:c.1121-91_1121-88del (HSPA8)	XP_011541100.1:n.1121-91_1121-88del
NM_006597.6:c.1121-91_1121-88del (HSPA8) MANE Select	NP_006588.1:n.1121-91_1121-88del
NM_153201.4:c.1121-91_1121-88del (HSPA8)	NP_694881.1:n.1121-91_1121-88del