Canonical Allele Identifier: CA339637732

Gene: LCK

Linked Data

• gnomAD v4: 1-32275955-G-C
• MyVariant Identifiers: chr1:g.32741556G>C (hg19) ; chr1:g.32275955G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32275955G>C , CM000663.2:g.32275955G>C	GRCh38
NC_000001.10:g.32741556G>C , CM000663.1:g.32741556G>C	GRCh37
NC_000001.9:g.32514143G>C	NCBI36
NG_023387.1:g.29717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355928.8:n.1046G>C
ENST00000482949.6:c.697G>C	ENSP00000431517.2:p.Gly233Arg
ENST00000495610.7:c.523G>C	ENSP00000435605.2:p.Gly175Arg
ENST00000696990.1:c.*213G>C	ENSP00000513026.1:n.*213G>C
ENST00000696991.1:c.121G>C
ENST00000336890.10:c.523G>C MANE Select	ENSP00000337825.5:p.Gly175Arg
ENST00000333070.4:c.523G>C	ENSP00000328213.4:p.Gly175Arg
ENST00000336890.9:c.523G>C	ENSP00000337825.5:p.Gly175Arg
ENST00000373557.6:c.655G>C	ENSP00000362658.2:p.Gly219Arg
ENST00000373564.7:c.697G>C	ENSP00000362665.3:p.Gly233Arg
ENST00000469765.5:n.582G>C
ENST00000469956.1:n.95G>C
ENST00000495610.6:c.523G>C	ENSP00000435605.1:p.Gly175Arg
ENST00000619559.4:c.523G>C	ENSP00000477713.1:p.Gly175Arg
NM_001042771.2:c.523G>C	NP_001036236.1:p.Gly175Arg
NM_005356.4:c.523G>C	NP_005347.3:p.Gly175Arg
XM_011541453.1:c.697G>C	XP_011539755.1:p.Gly233Arg
XM_011541454.1:c.697G>C	XP_011539756.1:p.Gly233Arg
XM_011541455.1:c.523G>C	XP_011539757.1:p.Gly175Arg
NM_001330468.1:c.523G>C	NP_001317397.1:p.Gly175Arg
XM_011541453.3:c.697G>C	XP_011539755.1:p.Gly233Arg
XM_024447046.1:c.697G>C	XP_024302814.1:p.Gly233Arg
XM_024447047.1:c.697G>C	XP_024302815.1:p.Gly233Arg
NM_005356.5:c.523G>C MANE Select	NP_005347.3:p.Gly175Arg
NM_001330468.2:c.523G>C	NP_001317397.1:p.Gly175Arg
NM_001042771.3:c.523G>C	NP_001036236.1:p.Gly175Arg