Canonical Allele Identifier: CA477385433

Gene: HSPA8 SNORD14D

Linked Data

• dbSNP Id: rs2135440657
• gnomAD v4: 11-123058922-C-T
• MyVariant Identifiers: chr11:g.122929630C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058922C>T , CM000673.2:g.123058922C>T	GRCh38
NC_000011.9:g.122929630C>T , CM000673.1:g.122929630C>T	GRCh37
NC_000011.8:g.122434840C>T	NCBI36
NG_029473.1:g.8215G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.1324-92G>A (HSPA8) MANE Select	ENSP00000432083.1:n.1324-92G>A
ENST00000227378.7:c.1324-92G>A (HSPA8)	ENSP00000227378.3:n.1324-92G>A
ENST00000453788.6:c.1324-92G>A (HSPA8)	ENSP00000404372.2:n.1324-92G>A
ENST00000524552.5:c.97-92G>A (HSPA8)	ENSP00000435908.1:n.97-92G>A
ENST00000526110.5:c.1267-92G>A (HSPA8)	ENSP00000433584.1:n.1267-92G>A
ENST00000526686.1:c.-113G>A (HSPA8)	ENSP00000435019.1:n.-113G>A
ENST00000532091.1:n.1207G>A (HSPA8)
ENST00000532636.5:c.1324-92G>A (HSPA8)	ENSP00000437125.1:n.1324-92G>A
ENST00000533238.5:n.426-92G>A (HSPA8)
ENST00000533540.5:c.886-92G>A (HSPA8)	ENSP00000437189.1:n.886-92G>A
ENST00000534319.5:c.616-92G>A (HSPA8)	ENSP00000433316.1:n.616-92G>A
ENST00000534624.5:c.1324-92G>A (HSPA8)	ENSP00000432083.1:n.1324-92G>A
NM_006597.5:c.1324-92G>A (HSPA8)	NP_006588.1:n.1324-92G>A
NM_153201.3:c.1324-92G>A (HSPA8)	NP_694881.1:n.1324-92G>A
NR_001454.2:n.74G>A (SNORD14D)
XM_011542798.1:c.1324-92G>A (HSPA8)	XP_011541100.1:n.1324-92G>A
NM_006597.6:c.1324-92G>A (HSPA8) MANE Select	NP_006588.1:n.1324-92G>A
NM_153201.4:c.1324-92G>A (HSPA8)	NP_694881.1:n.1324-92G>A