Canonical Allele Identifier: CA522361867

Gene: LCK

Linked Data

• ClinVar Variation Id: 2163521
• ClinVar RCV Id: RCV003092366
• dbSNP Id: rs1253746457
• gnomAD v2: 1-32741287-G-T
• gnomAD v3: 1-32275686-G-T
• gnomAD v4: 1-32275686-G-T
• MyVariant Identifiers: chr1:g.32741287G>T (hg19) ; chr1:g.32275686G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32275686G>T , CM000663.2:g.32275686G>T	GRCh38
NC_000001.10:g.32741287G>T , CM000663.1:g.32741287G>T	GRCh37
NC_000001.9:g.32513874G>T	NCBI36
NG_023387.1:g.29448G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355928.8:n.1004+14G>T
ENST00000482949.6:c.655+14G>T	ENSP00000431517.2:n.655+14G>T
ENST00000495610.7:c.481+14G>T	ENSP00000435605.2:n.481+14G>T
ENST00000696990.1:c.*171+14G>T	ENSP00000513026.1:n.*171+14G>T
ENST00000696991.1:c.114+14G>T
ENST00000336890.10:c.481+14G>T MANE Select	ENSP00000337825.5:n.481+14G>T
ENST00000333070.4:c.481+14G>T	ENSP00000328213.4:n.481+14G>T
ENST00000336890.9:c.481+14G>T	ENSP00000337825.5:n.481+14G>T
ENST00000373557.6:c.613+14G>T	ENSP00000362658.2:n.613+14G>T
ENST00000373564.7:c.655+14G>T	ENSP00000362665.3:n.655+14G>T
ENST00000469765.5:n.540+14G>T
ENST00000469956.1:n.53+14G>T
ENST00000495610.6:c.481+14G>T	ENSP00000435605.1:n.481+14G>T
ENST00000619559.4:c.481+14G>T	ENSP00000477713.1:n.481+14G>T
NM_001042771.2:c.481+14G>T	NP_001036236.1:n.481+14G>T
NM_005356.4:c.481+14G>T	NP_005347.3:n.481+14G>T
XM_011541453.1:c.655+14G>T	XP_011539755.1:n.655+14G>T
XM_011541454.1:c.655+14G>T	XP_011539756.1:n.655+14G>T
XM_011541455.1:c.481+14G>T	XP_011539757.1:n.481+14G>T
NM_001330468.1:c.481+14G>T	NP_001317397.1:n.481+14G>T
XM_011541453.3:c.655+14G>T	XP_011539755.1:n.655+14G>T
XM_024447046.1:c.655+14G>T	XP_024302814.1:n.655+14G>T
XM_024447047.1:c.655+14G>T	XP_024302815.1:n.655+14G>T
NM_005356.5:c.481+14G>T MANE Select	NP_005347.3:n.481+14G>T
NM_001330468.2:c.481+14G>T	NP_001317397.1:n.481+14G>T
NM_001042771.3:c.481+14G>T	NP_001036236.1:n.481+14G>T