Canonical Allele Identifier: CA366423886

Gene: TTLL2

Linked Data

• dbSNP Id: rs752600600
• MyVariant Identifiers: chr6:g.167754519T>G (hg19) ; chr6:g.167341031T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341031T>G , CM000668.2:g.167341031T>G	GRCh38
NC_000006.11:g.167754519T>G , CM000668.1:g.167754519T>G	GRCh37
NC_000006.10:g.167674509T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1131T>G MANE Select	ENSP00000239587.5:p.Asp377Glu
ENST00000649884.1:c.912T>G	ENSP00000497040.1:p.Asp304Glu
ENST00000239587.9:c.1131T>G	ENSP00000239587.5:p.Asp377Glu
ENST00000515138.1:c.1131T>G	ENSP00000424130.1:p.Asp377Glu
NM_031949.4:c.1131T>G	NP_114155.4:p.Asp377Glu
XM_006715572.2:c.912T>G	XP_006715635.1:p.Asp304Glu
XM_006715572.4:c.912T>G	XP_006715635.1:p.Asp304Glu
NM_031949.5:c.1131T>G MANE Select	NP_114155.4:p.Asp377Glu