Canonical Allele Identifier: CA2773968271

Gene: TTLL2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341109_167341110insTGTTTGGTTTTTGTTTGTGGC , CM000668.2:g.167341109_167341110insTGTTTGGTTTTTGTTTGTGGC	GRCh38
NC_000006.11:g.167754597_167754598insTGTTTGGTTTTTGTTTGTGGC , CM000668.1:g.167754597_167754598insTGTTTGGTTTTTGTTTGTGGC	GRCh37
NC_000006.10:g.167674587_167674588insTGTTTGGTTTTTGTTTGTGGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1209_1210insTGTTTGGTTTTTGTTTGTGGC MANE Select	ENSP00000239587.5:p.Val403_Lys404insCysLeuValPheValCysGly
ENST00000649884.1:c.990_991insTGTTTGGTTTTTGTTTGTGGC	ENSP00000497040.1:p.Val330_Lys331insCysLeuValPheValCysGly
ENST00000239587.9:c.1209_1210insTGTTTGGTTTTTGTTTGTGGC	ENSP00000239587.5:p.Val403_Lys404insCysLeuValPheValCysGly
ENST00000515138.1:c.1209_1210insTGTTTGGTTTTTGTTTGTGGC	ENSP00000424130.1:p.Val403_Lys404insCysLeuValPheValCysGly
NM_031949.4:c.1209_1210insTGTTTGGTTTTTGTTTGTGGC	NP_114155.4:p.Val403_Lys404insCysLeuValPheValCysGly
XM_006715572.2:c.990_991insTGTTTGGTTTTTGTTTGTGGC	XP_006715635.1:p.Val330_Lys331insCysLeuValPheValCysGly
XM_006715572.4:c.990_991insTGTTTGGTTTTTGTTTGTGGC	XP_006715635.1:p.Val330_Lys331insCysLeuValPheValCysGly
NM_031949.5:c.1209_1210insTGTTTGGTTTTTGTTTGTGGC MANE Select	NP_114155.4:p.Val403_Lys404insCysLeuValPheValCysGly