Canonical Allele Identifier: CA366424091
Gene: TTLL2 HGNC NCBI

Linked Data

dbSNP Id: rs1779085830

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167341122G>C , CM000668.2:g.167341122G>C GRCh38
NC_000006.11:g.167754610G>C , CM000668.1:g.167754610G>C GRCh37
NC_000006.10:g.167674600G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000239587.10:c.1222G>C MANE Select ENSP00000239587.5:p.Val408Leu
ENST00000649884.1:c.1003G>C ENSP00000497040.1:p.Val335Leu
ENST00000239587.9:c.1222G>C ENSP00000239587.5:p.Val408Leu
ENST00000515138.1:c.1222G>C ENSP00000424130.1:p.Val408Leu
NM_031949.4:c.1222G>C NP_114155.4:p.Val408Leu
XM_006715572.2:c.1003G>C XP_006715635.1:p.Val335Leu
XM_006715572.4:c.1003G>C XP_006715635.1:p.Val335Leu
NM_031949.5:c.1222G>C MANE Select NP_114155.4:p.Val408Leu