Canonical Allele Identifier: CA112105213

Gene: TENM3

Linked Data

• dbSNP Id: rs781567814
• gnomAD v2: 4-183200171-G-A
• gnomAD v3: 4-182279018-G-A
• gnomAD v4: 4-182279018-G-A
• MyVariant Identifiers: chr4:g.183200171G>A (hg19) ; chr4:g.182279018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182279018G>A , CM000666.2:g.182279018G>A	GRCh38
NC_000004.11:g.183200171G>A , CM000666.1:g.183200171G>A	GRCh37
NC_000004.10:g.183437165G>A	NCBI36
NG_042859.1:g.40588G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.-76+35542G>A MANE Select	ENSP00000424226.1:n.-76+35542G>A
ENST00000511685.5:c.-76+35542G>A	ENSP00000424226.1:n.-76+35542G>A
ENST00000512480.5:c.-75-44928G>A	ENSP00000421320.1:n.-75-44928G>A
ENST00000513201.1:n.176-44928G>A
NM_001080477.3:c.-76+35542G>A	NP_001073946.1:n.-76+35542G>A
XM_017008385.1:c.-75-44928G>A	XP_016863874.1:n.-75-44928G>A
XM_017008386.1:c.-75-44928G>A	XP_016863875.1:n.-75-44928G>A
XM_017008387.2:c.-75-44928G>A	XP_016863876.1:n.-75-44928G>A
XM_017008389.1:c.-75-44928G>A	XP_016863878.1:n.-75-44928G>A
XM_017008390.1:c.-75-44928G>A	XP_016863879.1:n.-75-44928G>A
XM_017008391.1:c.-75-44928G>A	XP_016863880.1:n.-75-44928G>A
XM_017008392.1:c.-75-44928G>A	XP_016863881.1:n.-75-44928G>A
XM_017008393.1:c.-75-44928G>A	XP_016863882.1:n.-75-44928G>A
XM_017008394.1:c.-75-44928G>A	XP_016863883.1:n.-75-44928G>A
NM_001080477.4:c.-76+35542G>A MANE Select	NP_001073946.1:n.-76+35542G>A