Canonical Allele Identifier: CA453305059

Gene: TTLL2

Linked Data

• MyVariant Identifiers: chr6:g.167754603A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341115A>G , CM000668.2:g.167341115A>G	GRCh38
NC_000006.11:g.167754603A>G , CM000668.1:g.167754603A>G	GRCh37
NC_000006.10:g.167674593A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1215A>G MANE Select	ENSP00000239587.5:p.Arg405=
ENST00000649884.1:c.996A>G	ENSP00000497040.1:p.Arg332=
ENST00000239587.9:c.1215A>G	ENSP00000239587.5:p.Arg405=
ENST00000515138.1:c.1215A>G	ENSP00000424130.1:p.Arg405=
NM_031949.4:c.1215A>G	NP_114155.4:p.Arg405=
XM_006715572.2:c.996A>G	XP_006715635.1:p.Arg332=
XM_006715572.4:c.996A>G	XP_006715635.1:p.Arg332=
NM_031949.5:c.1215A>G MANE Select	NP_114155.4:p.Arg405=