Canonical Allele Identifier: CA18299381

Gene: HSPB7

Linked Data

• dbSNP Id: rs535692942
• gnomAD v3: 1-16016798-C-A
• gnomAD v4: 1-16016798-C-A
• MyVariant Identifiers: chr1:g.16343293C>A (hg19) ; chr1:g.16016798C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16016798C>A , CM000663.2:g.16016798C>A	GRCh38
NC_000001.10:g.16343293C>A , CM000663.1:g.16343293C>A	GRCh37
NC_000001.9:g.16215880C>A	NCBI36
NG_053133.1:g.6999G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000311890.14:c.333+276G>T MANE Select	ENSP00000310111.9:n.333+276G>T
ENST00000311890.13:c.333+276G>T	ENSP00000310111.9:n.333+276G>T
ENST00000375718.4:c.558+276G>T	ENSP00000364870.4:n.558+276G>T
ENST00000406363.2:c.345+276G>T	ENSP00000385472.2:n.345+276G>T
ENST00000411503.5:c.318+291G>T	ENSP00000391578.1:n.318+291G>T
ENST00000442459.2:n.970+276G>T
ENST00000463576.5:c.195+291G>T	ENSP00000417966.1:n.195+291G>T
ENST00000487046.1:c.348+276G>T	ENSP00000419477.1:n.348+276G>T
NM_014424.4:c.333+276G>T	NP_055239.1:n.333+276G>T
XM_011541249.1:c.612+276G>T	XP_011539551.1:n.612+276G>T
XM_011541250.1:c.609+276G>T	XP_011539552.1:n.609+276G>T
NM_001349682.1:c.558+276G>T	NP_001336611.1:n.558+276G>T
NM_001349683.1:c.345+276G>T	NP_001336612.1:n.345+276G>T
NM_001349685.1:c.315+276G>T	NP_001336614.1:n.315+276G>T
NM_001349686.1:c.333+276G>T	NP_001336615.1:n.333+276G>T
NM_001349687.1:c.318+291G>T	NP_001336616.1:n.318+291G>T
NM_001349688.1:c.330+291G>T	NP_001336617.1:n.330+291G>T
NM_001349689.1:c.348+276G>T	NP_001336618.1:n.348+276G>T
NM_001349682.2:c.558+276G>T	NP_001336611.1:n.558+276G>T
NM_001349683.2:c.345+276G>T	NP_001336612.1:n.345+276G>T
NM_001349685.2:c.315+276G>T	NP_001336614.1:n.315+276G>T
NM_001349686.2:c.333+276G>T	NP_001336615.1:n.333+276G>T
NM_001349687.2:c.318+291G>T	NP_001336616.1:n.318+291G>T
NM_001349688.2:c.330+291G>T	NP_001336617.1:n.330+291G>T
NM_001349689.2:c.348+276G>T	NP_001336618.1:n.348+276G>T
NM_014424.5:c.333+276G>T MANE Select	NP_055239.1:n.333+276G>T