Canonical Allele Identifier: CA339636740

Gene: LCK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32275082C>T , CM000663.2:g.32275082C>T	GRCh38
NC_000001.10:g.32740683C>T , CM000663.1:g.32740683C>T	GRCh37
NC_000001.9:g.32513270C>T	NCBI36
NG_023387.1:g.28844C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005356.5:c.277C>T MANE Select	NP_005347.3:p.Gln93Ter
ENST00000336890.10:c.277C>T MANE Select	ENSP00000337825.5:p.Gln93Ter
NM_001042771.2:c.277C>T	NP_001036236.1:p.Gln93Ter
NM_001042771.3:c.277C>T	NP_001036236.1:p.Gln93Ter
NM_001330468.1:c.277C>T	NP_001317397.1:p.Gln93Ter
NM_001330468.2:c.277C>T	NP_001317397.1:p.Gln93Ter
NM_005356.4:c.277C>T	NP_005347.3:p.Gln93Ter
ENST00000333070.4:c.277C>T	ENSP00000328213.4:p.Gln93Ter
ENST00000336890.9:c.277C>T	ENSP00000337825.5:p.Gln93Ter
ENST00000355928.7:n.553C>T
ENST00000355928.8:n.563C>T
ENST00000373557.6:c.409C>T	ENSP00000362658.2:p.Gln137Ter
ENST00000373562.7:c.277C>T	ENSP00000362663.3:p.Gln93Ter
ENST00000373564.7:c.451C>T	ENSP00000362665.3:p.Gln151Ter
ENST00000469765.5:n.336C>T
ENST00000476457.5:n.356C>T
ENST00000482949.5:c.451C>T	ENSP00000431517.1:p.Gln151Ter
ENST00000482949.6:c.451C>T	ENSP00000431517.2:p.Gln151Ter
ENST00000495610.6:c.277C>T	ENSP00000435605.1:p.Gln93Ter
ENST00000495610.7:c.277C>T	ENSP00000435605.2:p.Gln93Ter
ENST00000619559.4:c.277C>T	ENSP00000477713.1:p.Gln93Ter
ENST00000696990.1:c.188-239C>T	ENSP00000513026.1:n.188-239C>T
XM_011541453.1:c.451C>T	XP_011539755.1:p.Gln151Ter
XM_011541453.3:c.451C>T	XP_011539755.1:p.Gln151Ter
XM_011541454.1:c.451C>T	XP_011539756.1:p.Gln151Ter
XM_011541455.1:c.277C>T	XP_011539757.1:p.Gln93Ter
XM_024447046.1:c.451C>T	XP_024302814.1:p.Gln151Ter
XM_024447047.1:c.451C>T	XP_024302815.1:p.Gln151Ter