Canonical Allele Identifier: CA3148205

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182743369T>C , CM000666.2:g.182743369T>C	GRCh38
NC_000004.11:g.183664522T>C , CM000666.1:g.183664522T>C	GRCh37
NC_000004.10:g.183901516T>C	NCBI36
NG_042859.1:g.504939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511685.6:c.3579T>C MANE Select	ENSP00000424226.1:p.Tyr1193=
ENST00000406950.3:c.3069T>C	ENSP00000385276.3:p.Tyr1023=
ENST00000502950.1:n.1966T>C
ENST00000511685.5:c.3579T>C	ENSP00000424226.1:p.Tyr1193=
NM_001080477.2:c.3579T>C	NP_001073946.1:p.Tyr1193=
NM_001080477.3:c.3579T>C	NP_001073946.1:p.Tyr1193=
XM_011532105.1:c.2808T>C	XP_011530407.1:p.Tyr936=
XM_017008385.1:c.3606T>C	XP_016863874.1:p.Tyr1202=
XM_017008386.1:c.3606T>C	XP_016863875.1:p.Tyr1202=
XM_017008387.2:c.3606T>C	XP_016863876.1:p.Tyr1202=
XM_017008388.1:c.3606T>C	XP_016863877.1:p.Tyr1202=
XM_017008389.1:c.3606T>C	XP_016863878.1:p.Tyr1202=
XM_017008390.1:c.3606T>C	XP_016863879.1:p.Tyr1202=
XM_017008391.1:c.3606T>C	XP_016863880.1:p.Tyr1202=
XM_017008392.1:c.3579T>C	XP_016863881.1:p.Tyr1193=
XM_017008393.1:c.3579T>C	XP_016863882.1:p.Tyr1193=
XM_017008394.1:c.3327T>C	XP_016863883.1:p.Tyr1109=
XM_017008395.1:c.3114T>C	XP_016863884.1:p.Tyr1038=
XM_017008396.1:c.2790T>C	XP_016863885.1:p.Tyr930=
NM_001080477.4:c.3579T>C MANE Select	NP_001073946.1:p.Tyr1193=