Canonical Allele Identifier: CA1307221957

Gene: TLK1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171134461C= , CM000664.2:g.171134461C=	GRCh38
NC_000002.11:g.171990971C= , CM000664.1:g.171990971C=	GRCh37
NC_000002.10:g.171699217C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012290.5:c.140-16604G= MANE Select	NP_036422.3:n.140-16604G=
ENST00000431350.7:c.140-16604G= MANE Select	ENSP00000411099.2:n.140-16604G=
NM_001136554.1:c.-5-16604G=	NP_001130026.1:n.-5-16604G=
NM_001136554.2:c.-5-16604G=	NP_001130026.1:n.-5-16604G=
NM_012290.4:c.140-16604G=	NP_036422.3:n.140-16604G=
ENST00000359766.7:c.140-16604G=	ENSP00000352810.3:n.140-16604G=
ENST00000360843.7:c.140-16604G=	ENSP00000354089.3:n.140-16604G=
ENST00000409443.6:c.140-16604G=	ENSP00000387313.2:n.140-16604G=
ENST00000413010.5:n.276-16604G=
ENST00000431350.6:c.140-16604G=	ENSP00000411099.2:n.140-16604G=
ENST00000466220.1:n.241-16604G=
ENST00000470340.1:n.331-16604G=
ENST00000521943.5:c.-5-16604G=	ENSP00000428113.1:n.-5-16604G=
XM_011512238.1:c.140-16604G=	XP_011510540.1:n.140-16604G=
XM_011512238.3:c.140-16604G=	XP_011510540.1:n.140-16604G=
XM_017005422.2:c.-394+25829G=	XP_016860911.1:n.-394+25829G=
XR_001739084.2:n.527-16604G=
XR_001739085.2:n.527-16604G=
XR_923070.1:n.652-16604G=