Canonical Allele Identifier: CA1139848750

Gene: HSPB7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16014456A= , CM000663.2:g.16014456A=	GRCh38
NC_000001.10:g.16340951A= , CM000663.1:g.16340951A=	GRCh37
NC_000001.9:g.16213538A=	NCBI36
NG_053133.1:g.9341T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311890.14:c.*1124T= MANE Select	ENSP00000310111.9:n.*1124T=
ENST00000311890.13:c.*1124T=	ENSP00000310111.9:n.*1124T=
ENST00000375718.4:c.*1124T=	ENSP00000364870.4:n.*1124T=
ENST00000411503.5:c.*1124T=	ENSP00000391578.1:n.*1124T=
ENST00000442459.2:n.2274T=
NM_014424.4:c.*1124T=	NP_055239.1:n.*1124T=
XM_011541249.1:c.*1124T=	XP_011539551.1:n.*1124T=
XM_011541250.1:c.*1124T=	XP_011539552.1:n.*1124T=
NM_001349682.1:c.*1124T=	NP_001336611.1:n.*1124T=
NM_001349683.1:c.*1124T=	NP_001336612.1:n.*1124T=
NM_001349685.1:c.*1124T=	NP_001336614.1:n.*1124T=
NM_001349686.1:c.*1124T=	NP_001336615.1:n.*1124T=
NM_001349687.1:c.*1124T=	NP_001336616.1:n.*1124T=
NM_001349688.1:c.*1124T=	NP_001336617.1:n.*1124T=
NM_001349689.1:c.*1124T=	NP_001336618.1:n.*1124T=
NM_001349682.2:c.*1124T=	NP_001336611.1:n.*1124T=
NM_001349683.2:c.*1124T=	NP_001336612.1:n.*1124T=
NM_001349685.2:c.*1124T=	NP_001336614.1:n.*1124T=
NM_001349686.2:c.*1124T=	NP_001336615.1:n.*1124T=
NM_001349687.2:c.*1124T=	NP_001336616.1:n.*1124T=
NM_001349688.2:c.*1124T=	NP_001336617.1:n.*1124T=
NM_001349689.2:c.*1124T=	NP_001336618.1:n.*1124T=
NM_014424.5:c.*1124T= MANE Select	NP_055239.1:n.*1124T=