Canonical Allele Identifier: CA1718330678
Gene: HSPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303763C= , CM000669.2:g.76303763C= GRCh38
NC_000007.13:g.75933080C= , CM000669.1:g.75933080C= GRCh37
NC_000007.12:g.75771016C= NCBI36
NG_008995.1:g.6206C= , LRG_248:g.6206C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248553.7:c.365-39C= MANE Select ENSP00000248553.6:n.365-39C=
ENST00000674547.1:c.365-39C= ENSP00000502461.1:n.365-39C=
ENST00000674638.1:c.365-44C= ENSP00000502651.1:n.365-44C=
ENST00000674650.1:c.365-221C= ENSP00000501628.1:n.365-221C=
ENST00000674965.1:c.365-14C= ENSP00000501765.1:n.365-14C=
ENST00000675134.1:c.365-39C= ENSP00000501831.1:n.365-39C=
ENST00000675226.1:c.369-44C= ENSP00000502510.1:n.369-44C=
ENST00000675417.1:n.559C=
ENST00000675538.1:c.400-39C= ENSP00000502495.1:n.400-39C=
ENST00000675733.1:n.406C=
ENST00000675906.1:c.365-39C= ENSP00000502714.1:n.365-39C=
ENST00000676195.1:n.81-39C=
ENST00000676231.1:c.394+36C= ENSP00000502249.1:n.394+36C=
ENST00000248553.6:c.365-39C= ENSP00000248553.6:n.365-39C=
ENST00000429938.1:c.-141+36C= ENSP00000405285.1:n.-141+36C=
ENST00000447574.1:c.*490C= ENSP00000414357.1:n.*490C=
NM_001540.3:c.365-39C= , LRG_248t1:c.365-39C= NP_001531.1:n.365-39C=
NM_001540.4:c.365-39C= NP_001531.1:n.365-39C=
NM_001540.5:c.365-39C= MANE Select NP_001531.1:n.365-39C=