Canonical Allele Identifier: CA366423937

Gene: TTLL2

Linked Data

• COSMIC: COSM3860415
• MyVariant Identifiers: chr6:g.167754541T>G (hg19) ; chr6:g.167341053T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341053T>G , CM000668.2:g.167341053T>G	GRCh38
NC_000006.11:g.167754541T>G , CM000668.1:g.167754541T>G	GRCh37
NC_000006.10:g.167674531T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1153T>G MANE Select	ENSP00000239587.5:p.Leu385Val
ENST00000649884.1:c.934T>G	ENSP00000497040.1:p.Leu312Val
ENST00000239587.9:c.1153T>G	ENSP00000239587.5:p.Leu385Val
ENST00000515138.1:c.1153T>G	ENSP00000424130.1:p.Leu385Val
NM_031949.4:c.1153T>G	NP_114155.4:p.Leu385Val
XM_006715572.2:c.934T>G	XP_006715635.1:p.Leu312Val
XM_006715572.4:c.934T>G	XP_006715635.1:p.Leu312Val
NM_031949.5:c.1153T>G MANE Select	NP_114155.4:p.Leu385Val