Canonical Allele Identifier: CA453304994

Gene: TTLL2

Linked Data

• MyVariant Identifiers: chr6:g.167754564C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341076C>G , CM000668.2:g.167341076C>G	GRCh38
NC_000006.11:g.167754564C>G , CM000668.1:g.167754564C>G	GRCh37
NC_000006.10:g.167674554C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1176C>G MANE Select	ENSP00000239587.5:p.Ala392=
ENST00000649884.1:c.957C>G	ENSP00000497040.1:p.Ala319=
ENST00000239587.9:c.1176C>G	ENSP00000239587.5:p.Ala392=
ENST00000515138.1:c.1176C>G	ENSP00000424130.1:p.Ala392=
NM_031949.4:c.1176C>G	NP_114155.4:p.Ala392=
XM_006715572.2:c.957C>G	XP_006715635.1:p.Ala319=
XM_006715572.4:c.957C>G	XP_006715635.1:p.Ala319=
NM_031949.5:c.1176C>G MANE Select	NP_114155.4:p.Ala392=