Canonical Allele Identifier: CA335090187
Community Standard Title: NM_001163278.2(TENM1):c.6076+299G>T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124385378C>A , CM000685.2:g.124385378C>A GRCh38
NC_000023.10:g.123519228C>A , CM000685.1:g.123519228C>A GRCh37
NC_000023.9:g.123346909C>A NCBI36
NG_013249.1:g.583439G>T
NG_033796.2:g.429819C>A , LRG_782:g.429819C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001163278.2:c.6076+299G>T (TENM1) MANE Select NP_001156750.1:n.6076+299G>T
ENST00000422452.4:c.6076+299G>T (TENM1) MANE Select ENSP00000403954.4:n.6076+299G>T
NM_001163278.1:c.6076+299G>T (TENM1) NP_001156750.1:n.6076+299G>T
NM_001163279.1:c.6073+299G>T (TENM1) NP_001156751.1:n.6073+299G>T
NM_014253.3:c.6055+299G>T (TENM1) NP_055068.2:n.6055+299G>T
ENST00000371130.7:c.6055+299G>T (TENM1) ENSP00000360171.3:n.6055+299G>T
ENST00000422452.2:c.6076+299G>T (TENM1) ENSP00000403954.2:n.6076+299G>T
ENST00000422452.3:c.6022+299G>T (TENM1) ENSP00000403954.3:n.6022+299G>T
ENST00000469481.1:n.454-26444C>A (STAG2)
XM_011531230.1:c.6076+299G>T (TENM1) XP_011529532.1:n.6076+299G>T
XM_011531230.3:c.6076+299G>T (TENM1) XP_011529532.1:n.6076+299G>T
XM_011531231.1:c.6076+299G>T (TENM1) XP_011529533.1:n.6076+299G>T
XM_011531232.1:c.6076+299G>T (TENM1) XP_011529534.1:n.6076+299G>T
XM_011531233.1:c.6076+299G>T (TENM1) XP_011529535.1:n.6076+299G>T
XM_011531234.1:c.6076+299G>T (TENM1) XP_011529536.1:n.6076+299G>T
XM_011531235.1:c.4852+299G>T (TENM1) XP_011529537.1:n.4852+299G>T
XM_011531236.1:c.2191+299G>T (TENM1) XP_011529538.1:n.2191+299G>T
XM_011531236.3:c.3781+299G>T (TENM1) XP_011529538.2:n.3781+299G>T
XM_011531237.1:c.2080+299G>T (TENM1) XP_011529539.1:n.2080+299G>T
XM_011531237.3:c.2080+299G>T (TENM1) XP_011529539.1:n.2080+299G>T
XM_017029208.2:c.6175+299G>T (TENM1) XP_016884697.1:n.6175+299G>T
XM_017029209.2:c.6175+299G>T (TENM1) XP_016884698.1:n.6175+299G>T
XM_017029210.2:c.6175+299G>T (TENM1) XP_016884699.1:n.6175+299G>T
XM_017029211.2:c.6175+299G>T (TENM1) XP_016884700.1:n.6175+299G>T
XM_017029212.2:c.6175+299G>T (TENM1) XP_016884701.1:n.6175+299G>T
XM_017029213.2:c.6175+299G>T (TENM1) XP_016884702.1:n.6175+299G>T
XM_017029214.2:c.6055+299G>T (TENM1) XP_016884703.1:n.6055+299G>T
XR_938576.1:n.89-2411C>A