Canonical Allele Identifier: CA7599152
Gene: TLN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.62708694C>T , CM000677.2:g.62708694C>T GRCh38
NC_000015.9:g.63000893C>T , CM000677.1:g.63000893C>T GRCh37
NC_000015.8:g.60788185C>T NCBI36
NG_033932.1:g.66384C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015059.3:c.2365C>T MANE Select NP_055874.2:p.Arg789Trp
ENST00000636159.2:c.2365C>T MANE Select ENSP00000490662.2:p.Arg789Trp
NM_001394547.1:c.2365C>T NP_001381476.1:p.Arg789Trp
NM_015059.2:c.2365C>T NP_055874.2:p.Arg789Trp
ENST00000306829.10:c.2365C>T ENSP00000303476.6:p.Arg789Trp
ENST00000561311.5:c.2365C>T ENSP00000453508.1:p.Arg789Trp
ENST00000636159.1:c.92-13684C>T ENSP00000490662.1:n.92-13684C>T
XM_005254707.1:c.2365C>T XP_005254764.1:p.Arg789Trp
XM_005254708.3:c.2365C>T XP_005254765.1:p.Arg789Trp
XM_005254708.4:c.2365C>T XP_005254765.1:p.Arg789Trp
XM_005254710.3:c.2365C>T XP_005254767.1:p.Arg789Trp
XM_005254710.5:c.2365C>T XP_005254767.1:p.Arg789Trp
XM_005254711.3:c.2365C>T XP_005254768.1:p.Arg789Trp
XM_005254711.5:c.2365C>T XP_005254768.1:p.Arg789Trp
XM_005254712.3:c.2365C>T XP_005254769.1:p.Arg789Trp
XM_005254712.4:c.2365C>T XP_005254769.1:p.Arg789Trp
XM_005254713.3:c.2365C>T XP_005254770.1:p.Arg789Trp
XM_005254713.5:c.2365C>T XP_005254770.1:p.Arg789Trp
XM_005254714.2:c.2365C>T XP_005254771.1:p.Arg789Trp
XM_005254714.3:c.2365C>T XP_005254771.1:p.Arg789Trp
XM_005254715.1:c.2365C>T XP_005254772.1:p.Arg789Trp
XM_005254715.3:c.2365C>T XP_005254772.1:p.Arg789Trp
XM_006720717.2:c.2365C>T XP_006720780.1:p.Arg789Trp
XM_006720717.4:c.2365C>T XP_006720780.1:p.Arg789Trp
XM_011522106.1:c.2365C>T XP_011520408.1:p.Arg789Trp
XM_011522107.1:c.2365C>T XP_011520409.1:p.Arg789Trp
XM_011522108.1:c.2365C>T XP_011520410.1:p.Arg789Trp
XM_017022665.2:c.2365C>T XP_016878154.1:p.Arg789Trp
XM_017022666.1:c.2365C>T XP_016878155.1:p.Arg789Trp
XM_017022667.1:c.2365C>T XP_016878156.1:p.Arg789Trp
XM_017022668.2:c.2365C>T XP_016878157.1:p.Arg789Trp
XM_017022669.1:c.2365C>T XP_016878158.1:p.Arg789Trp
XM_024450087.1:c.2365C>T XP_024305855.1:p.Arg789Trp
XR_001751405.2:n.3473C>T
XR_931919.1:n.2673C>T