Canonical Allele Identifier: CA735011517

Gene: LCK

Linked Data

• ClinVar Variation Id: 2895395
• ClinVar RCV Id: RCV003746494
• dbSNP Id: rs1275429035
• gnomAD v3: 1-32275313-T-C
• gnomAD v4: 1-32275313-T-C
• MyVariant Identifiers: chr1:g.32740914T>C (hg19) ; chr1:g.32275313T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32275313T>C , CM000663.2:g.32275313T>C	GRCh38
NC_000001.10:g.32740914T>C , CM000663.1:g.32740914T>C	GRCh37
NC_000001.9:g.32513501T>C	NCBI36
NG_023387.1:g.29075T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355928.8:n.794T>C
ENST00000482949.6:c.453-8T>C	ENSP00000431517.2:n.453-8T>C
ENST00000495610.7:c.279-8T>C	ENSP00000435605.2:n.279-8T>C
ENST00000696990.1:c.188-8T>C	ENSP00000513026.1:n.188-8T>C
ENST00000336890.10:c.279-8T>C MANE Select	ENSP00000337825.5:n.279-8T>C
ENST00000333070.4:c.279-8T>C	ENSP00000328213.4:n.279-8T>C
ENST00000336890.9:c.279-8T>C	ENSP00000337825.5:n.279-8T>C
ENST00000373557.6:c.411-8T>C	ENSP00000362658.2:n.411-8T>C
ENST00000373562.7:c.279-8T>C	ENSP00000362663.3:n.279-8T>C
ENST00000373564.7:c.453-8T>C	ENSP00000362665.3:n.453-8T>C
ENST00000469765.5:n.338-8T>C
ENST00000476457.5:n.587T>C
ENST00000482949.5:c.453-8T>C	ENSP00000431517.1:n.453-8T>C
ENST00000495610.6:c.279-8T>C	ENSP00000435605.1:n.279-8T>C
ENST00000619559.4:c.279-8T>C	ENSP00000477713.1:n.279-8T>C
NM_001042771.2:c.279-8T>C	NP_001036236.1:n.279-8T>C
NM_005356.4:c.279-8T>C	NP_005347.3:n.279-8T>C
XM_011541453.1:c.453-8T>C	XP_011539755.1:n.453-8T>C
XM_011541454.1:c.453-8T>C	XP_011539756.1:n.453-8T>C
XM_011541455.1:c.279-8T>C	XP_011539757.1:n.279-8T>C
NM_001330468.1:c.279-8T>C	NP_001317397.1:n.279-8T>C
XM_011541453.3:c.453-8T>C	XP_011539755.1:n.453-8T>C
XM_024447046.1:c.453-8T>C	XP_024302814.1:n.453-8T>C
XM_024447047.1:c.453-8T>C	XP_024302815.1:n.453-8T>C
NM_005356.5:c.279-8T>C MANE Select	NP_005347.3:n.279-8T>C
NM_001330468.2:c.279-8T>C	NP_001317397.1:n.279-8T>C
NM_001042771.3:c.279-8T>C	NP_001036236.1:n.279-8T>C