Canonical Allele Identifier: CA366424128

Gene: TTLL2

Linked Data

• dbSNP Id: rs1221594316
• MyVariant Identifiers: chr6:g.167754626A>T (hg19) ; chr6:g.167341138A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341138A>T , CM000668.2:g.167341138A>T	GRCh38
NC_000006.11:g.167754626A>T , CM000668.1:g.167754626A>T	GRCh37
NC_000006.10:g.167674616A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1238A>T MANE Select	ENSP00000239587.5:p.Asp413Val
ENST00000649884.1:c.1019A>T	ENSP00000497040.1:p.Asp340Val
ENST00000239587.9:c.1238A>T	ENSP00000239587.5:p.Asp413Val
ENST00000515138.1:c.1238A>T	ENSP00000424130.1:p.Asp413Val
NM_031949.4:c.1238A>T	NP_114155.4:p.Asp413Val
XM_006715572.2:c.1019A>T	XP_006715635.1:p.Asp340Val
XM_006715572.4:c.1019A>T	XP_006715635.1:p.Asp340Val
NM_031949.5:c.1238A>T MANE Select	NP_114155.4:p.Asp413Val