Canonical Allele Identifier: CA453305259

Gene: TTLL2

Linked Data

• dbSNP Id: rs1325588151
• gnomAD v2: 6-167754693-C-T
• gnomAD v4: 6-167341205-C-T
• MyVariant Identifiers: chr6:g.167754693C>T (hg19) ; chr6:g.167341205C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167341205C>T , CM000668.2:g.167341205C>T	GRCh38
NC_000006.11:g.167754693C>T , CM000668.1:g.167754693C>T	GRCh37
NC_000006.10:g.167674683C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239587.10:c.1305C>T MANE Select	ENSP00000239587.5:p.Ser435=
ENST00000649884.1:c.1086C>T	ENSP00000497040.1:p.Ser362=
ENST00000239587.9:c.1305C>T	ENSP00000239587.5:p.Ser435=
ENST00000515138.1:c.1305C>T	ENSP00000424130.1:p.Ser435=
NM_031949.4:c.1305C>T	NP_114155.4:p.Ser435=
XM_006715572.2:c.1086C>T	XP_006715635.1:p.Ser362=
XM_006715572.4:c.1086C>T	XP_006715635.1:p.Ser362=
NM_031949.5:c.1305C>T MANE Select	NP_114155.4:p.Ser435=