Canonical Allele Identifier: CA740970

Gene: LCK

Linked Data

• ClinVar Variation Id: 541837
• ClinVar RCV Id: RCV001463974
• dbSNP Id: rs144437329
• ExAC: 1:32740014 C / T
• gnomAD v2: 1-32740014-C-T
• gnomAD v3: 1-32274413-C-T
• gnomAD v4: 1-32274413-C-T
• MyVariant Identifiers: chr1:g.32740014C>T (hg19) ; chr1:g.32274413C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32274413C>T , CM000663.2:g.32274413C>T	GRCh38
NC_000001.10:g.32740014C>T , CM000663.1:g.32740014C>T	GRCh37
NC_000001.9:g.32512601C>T	NCBI36
NG_023387.1:g.28175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355928.8:n.196C>T
ENST00000482949.6:c.84C>T	ENSP00000431517.2:p.Val28=
ENST00000495610.7:c.84C>T	ENSP00000435605.2:p.Val28=
ENST00000696990.1:c.84C>T	ENSP00000513026.1:p.Val28=
ENST00000336890.10:c.84C>T MANE Select	ENSP00000337825.5:p.Val28=
ENST00000333070.4:c.84C>T	ENSP00000328213.4:p.Val28=
ENST00000336890.9:c.84C>T	ENSP00000337825.5:p.Val28=
ENST00000355928.7:n.186C>T
ENST00000373557.6:c.216C>T	ENSP00000362658.2:p.Val72=
ENST00000373562.7:c.84C>T	ENSP00000362663.3:p.Val28=
ENST00000373564.7:c.84C>T	ENSP00000362665.3:p.Val28=
ENST00000461712.6:c.84C>T	ENSP00000434525.1:p.Val28=
ENST00000469765.5:n.143C>T
ENST00000476457.5:n.163C>T
ENST00000477031.6:c.216C>T	ENSP00000436554.1:p.Val72=
ENST00000482949.5:c.84C>T	ENSP00000431517.1:p.Val28=
ENST00000495610.6:c.84C>T	ENSP00000435605.1:p.Val28=
ENST00000619559.4:c.84C>T	ENSP00000477713.1:p.Val28=
NM_001042771.2:c.84C>T	NP_001036236.1:p.Val28=
NM_005356.4:c.84C>T	NP_005347.3:p.Val28=
XM_011541453.1:c.84C>T	XP_011539755.1:p.Val28=
XM_011541454.1:c.84C>T	XP_011539756.1:p.Val28=
XM_011541455.1:c.84C>T	XP_011539757.1:p.Val28=
NM_001330468.1:c.84C>T	NP_001317397.1:p.Val28=
XM_011541453.3:c.84C>T	XP_011539755.1:p.Val28=
XM_024447046.1:c.84C>T	XP_024302814.1:p.Val28=
XM_024447047.1:c.84C>T	XP_024302815.1:p.Val28=
NM_005356.5:c.84C>T MANE Select	NP_005347.3:p.Val28=
NM_001330468.2:c.84C>T	NP_001317397.1:p.Val28=
NM_001042771.3:c.84C>T	NP_001036236.1:p.Val28=