Canonical Allele Identifier: CA1155602881

Gene: HSPB7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16016673G= , CM000663.2:g.16016673G=	GRCh38
NC_000001.10:g.16343168G= , CM000663.1:g.16343168G=	GRCh37
NC_000001.9:g.16215755G=	NCBI36
NG_053133.1:g.7124C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311890.14:c.333+401C= MANE Select	ENSP00000310111.9:n.333+401C=
ENST00000311890.13:c.333+401C=	ENSP00000310111.9:n.333+401C=
ENST00000375718.4:c.558+401C=	ENSP00000364870.4:n.558+401C=
ENST00000406363.2:c.345+401C=	ENSP00000385472.2:n.345+401C=
ENST00000411503.5:c.318+416C=	ENSP00000391578.1:n.318+416C=
ENST00000442459.2:n.970+401C=
ENST00000463576.5:c.195+416C=	ENSP00000417966.1:n.195+416C=
ENST00000487046.1:c.348+401C=	ENSP00000419477.1:n.348+401C=
NM_014424.4:c.333+401C=	NP_055239.1:n.333+401C=
XM_011541249.1:c.612+401C=	XP_011539551.1:n.612+401C=
XM_011541250.1:c.609+401C=	XP_011539552.1:n.609+401C=
NM_001349682.1:c.558+401C=	NP_001336611.1:n.558+401C=
NM_001349683.1:c.345+401C=	NP_001336612.1:n.345+401C=
NM_001349685.1:c.315+401C=	NP_001336614.1:n.315+401C=
NM_001349686.1:c.333+401C=	NP_001336615.1:n.333+401C=
NM_001349687.1:c.318+416C=	NP_001336616.1:n.318+416C=
NM_001349688.1:c.330+416C=	NP_001336617.1:n.330+416C=
NM_001349689.1:c.348+401C=	NP_001336618.1:n.348+401C=
NM_001349682.2:c.558+401C=	NP_001336611.1:n.558+401C=
NM_001349683.2:c.345+401C=	NP_001336612.1:n.345+401C=
NM_001349685.2:c.315+401C=	NP_001336614.1:n.315+401C=
NM_001349686.2:c.333+401C=	NP_001336615.1:n.333+401C=
NM_001349687.2:c.318+416C=	NP_001336616.1:n.318+416C=
NM_001349688.2:c.330+416C=	NP_001336617.1:n.330+416C=
NM_001349689.2:c.348+401C=	NP_001336618.1:n.348+401C=
NM_014424.5:c.333+401C= MANE Select	NP_055239.1:n.333+401C=