Canonical Allele Identifier: CA272340014

Gene: TLN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.62395140C>G , CM000677.2:g.62395140C>G	GRCh38
NC_000015.9:g.62687339C>G , CM000677.1:g.62687339C>G	GRCh37
NC_000015.8:g.60474631C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636159.2:c.-238+4455C>G MANE Select	ENSP00000490662.2:n.-238+4455C>G
ENST00000561322.1:n.160+4455C>G
XM_005254708.3:c.-238+4455C>G	XP_005254765.1:n.-238+4455C>G
XM_005254710.3:c.-381+4455C>G	XP_005254767.1:n.-381+4455C>G
XM_005254711.3:c.-238+2729C>G	XP_005254768.1:n.-238+2729C>G
XM_005254714.2:c.-113+4455C>G	XP_005254771.1:n.-113+4455C>G
XM_011522106.1:c.-238+4455C>G	XP_011520408.1:n.-238+4455C>G
XM_011522107.1:c.-238+4455C>G	XP_011520409.1:n.-238+4455C>G
XM_011522108.1:c.-238+4455C>G	XP_011520410.1:n.-238+4455C>G
XR_931919.1:n.71+4455C>G
XM_005254708.4:c.-238+4455C>G	XP_005254765.1:n.-238+4455C>G
XM_005254710.5:c.-381+4455C>G	XP_005254767.1:n.-381+4455C>G
XM_005254711.5:c.-238+2729C>G	XP_005254768.1:n.-238+2729C>G
XM_005254714.3:c.-113+4455C>G	XP_005254771.1:n.-113+4455C>G
XM_024450087.1:c.-256+4455C>G	XP_024305855.1:n.-256+4455C>G
NM_001394547.1:c.-113+4455C>G	NP_001381476.1:n.-113+4455C>G
NM_015059.3:c.-238+4455C>G MANE Select	NP_055874.2:n.-238+4455C>G