Canonical Allele Identifier: CA448070127

Gene: SQSTM1

Linked Data

• MyVariant Identifiers: chr5:g.179260772T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.179833772T>C , CM000667.2:g.179833772T>C	GRCh38
NC_000005.9:g.179260772T>C , CM000667.1:g.179260772T>C	GRCh37
NC_000005.8:g.179193378T>C	NCBI36
NG_011342.1:g.32385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389805.9:c.1155T>C MANE Select	ENSP00000374455.4:p.His385=
ENST00000360718.5:c.903T>C	ENSP00000353944.5:p.His301=
ENST00000389805.8:c.1155T>C	ENSP00000374455.4:p.His385=
ENST00000510187.5:c.950+545T>C	ENSP00000424477.1:n.950+545T>C
NM_001142298.1:c.903T>C	NP_001135770.1:p.His301=
NM_001142299.1:c.903T>C	NP_001135771.1:p.His301=
NM_003900.4:c.1155T>C	NP_003891.1:p.His385=
XM_017010010.1:c.903T>C	XP_016865499.1:p.His301=
NM_003900.5:c.1155T>C MANE Select	NP_003891.1:p.His385=
NM_001142298.2:c.903T>C	NP_001135770.1:p.His301=
NM_001142299.2:c.903T>C	NP_001135771.1:p.His301=