Canonical Allele Identifier: CA575786744

Gene: HSPB1

Linked Data

• dbSNP Id: rs1563651927
• gnomAD v2: 7-75932234-G-GTGA
• gnomAD v4: 7-76302917-G-GTGA
• MyVariant Identifiers: chr7:g.75932234_75932235insTGA (hg19) ; chr7:g.76302917_76302918insTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.76302917_76302918insTGA , CM000669.2:g.76302917_76302918insTGA	GRCh38
NC_000007.13:g.75932234_75932235insTGA , CM000669.1:g.75932234_75932235insTGA	GRCh37
NC_000007.12:g.75770170_75770171insTGA	NCBI36
NG_008995.1:g.5360_5361insTGA , LRG_248:g.5360_5361insTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248553.7:c.205_206insTGA MANE Select	ENSP00000248553.6:p.Ala69delinsValThr
ENST00000674547.1:c.205_206insTGA	ENSP00000502461.1:p.Ala69delinsValThr
ENST00000674560.1:n.245_246insTGA
ENST00000674638.1:c.205_206insTGA	ENSP00000502651.1:p.Ala69delinsValThr
ENST00000674650.1:c.205_206insTGA	ENSP00000501628.1:p.Ala69delinsValThr
ENST00000674965.1:c.205_206insTGA	ENSP00000501765.1:p.Ala69delinsValThr
ENST00000675134.1:c.205_206insTGA	ENSP00000501831.1:p.Ala69delinsValThr
ENST00000675226.1:c.205_206insTGA	ENSP00000502510.1:p.Ala69delinsValThr
ENST00000675488.1:n.245_246insTGA
ENST00000675538.1:c.205_206insTGA	ENSP00000502495.1:p.Ala69delinsValThr
ENST00000675624.1:n.245_246insTGA
ENST00000675733.1:n.245_246insTGA
ENST00000675906.1:c.205_206insTGA	ENSP00000502714.1:p.Ala69delinsValThr
ENST00000676231.1:c.205_206insTGA	ENSP00000502249.1:p.Ala69delinsValThr
ENST00000676398.1:n.245_246insTGA
ENST00000248553.6:c.205_206insTGA	ENSP00000248553.6:p.Ala69delinsValThr
ENST00000447574.1:c.205_206insTGA	ENSP00000414357.1:p.Ala69delinsValThr
NM_001540.3:c.205_206insTGA , LRG_248t1:c.205_206insTGA	NP_001531.1:p.Ala69delinsValThr
NM_001540.4:c.205_206insTGA	NP_001531.1:p.Ala69delinsValThr
NM_001540.5:c.205_206insTGA MANE Select	NP_001531.1:p.Ala69delinsValThr