Canonical Allele Identifier: CA335335825
Gene: TENM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.124939813A>G , CM000685.2:g.124939813A>G GRCh38
NC_000023.10:g.124073662A>G , CM000685.1:g.124073662A>G GRCh37
NC_000023.9:g.123901343A>G NCBI36
NG_013249.1:g.29005T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000422452.4:c.217+23724T>C MANE Select ENSP00000403954.4:n.217+23724T>C
ENST00000422452.3:c.163+23724T>C ENSP00000403954.3:n.163+23724T>C
ENST00000371130.7:c.217+23724T>C ENSP00000360171.3:n.217+23724T>C
ENST00000422452.2:c.217+23724T>C ENSP00000403954.2:n.217+23724T>C
NM_001163278.1:c.217+23724T>C NP_001156750.1:n.217+23724T>C
NM_001163279.1:c.217+23724T>C NP_001156751.1:n.217+23724T>C
NM_014253.3:c.217+23724T>C NP_055068.2:n.217+23724T>C
XM_011531230.1:c.217+23724T>C XP_011529532.1:n.217+23724T>C
XM_011531231.1:c.217+23724T>C XP_011529533.1:n.217+23724T>C
XM_011531232.1:c.217+23724T>C XP_011529534.1:n.217+23724T>C
XM_011531233.1:c.217+23724T>C XP_011529535.1:n.217+23724T>C
XM_011531234.1:c.217+23724T>C XP_011529536.1:n.217+23724T>C
XM_011531230.3:c.217+23724T>C XP_011529532.1:n.217+23724T>C
XM_017029208.2:c.217+23724T>C XP_016884697.1:n.217+23724T>C
XM_017029209.2:c.217+23724T>C XP_016884698.1:n.217+23724T>C
XM_017029210.2:c.217+23724T>C XP_016884699.1:n.217+23724T>C
XM_017029211.2:c.217+23724T>C XP_016884700.1:n.217+23724T>C
XM_017029212.2:c.217+23724T>C XP_016884701.1:n.217+23724T>C
XM_017029213.2:c.217+23724T>C XP_016884702.1:n.217+23724T>C
XM_017029214.2:c.217+23724T>C XP_016884703.1:n.217+23724T>C
XM_017029215.2:c.217+23724T>C XP_016884704.1:n.217+23724T>C
XM_017029216.2:c.217+23724T>C XP_016884705.1:n.217+23724T>C
NM_001163278.2:c.217+23724T>C MANE Select NP_001156750.1:n.217+23724T>C
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