Canonical Allele Identifier: CA11670793

Gene: TENM3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182216245T>C , CM000666.2:g.182216245T>C	GRCh38
NC_000004.11:g.183137398T>C , CM000666.1:g.183137398T>C	GRCh37
NC_000004.10:g.183374392T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512480.5:c.-76+71491T>C	ENSP00000421320.1:n.-76+71491T>C
ENST00000513201.1:n.175+72084T>C
XR_939529.1:n.332+145A>G
XR_939530.1:n.332+145A>G
XM_017008385.1:c.-75-107701T>C	XP_016863874.1:n.-75-107701T>C
XM_017008386.1:c.-76+72084T>C	XP_016863875.1:n.-76+72084T>C
XM_017008387.2:c.-76+71491T>C	XP_016863876.1:n.-76+71491T>C
XM_017008389.1:c.-75-107701T>C	XP_016863878.1:n.-75-107701T>C
XM_017008390.1:c.-75-107701T>C	XP_016863879.1:n.-75-107701T>C
XM_017008391.1:c.-75-107701T>C	XP_016863880.1:n.-75-107701T>C
XM_017008392.1:c.-75-107701T>C	XP_016863881.1:n.-75-107701T>C
XM_017008393.1:c.-75-107701T>C	XP_016863882.1:n.-75-107701T>C
XM_017008394.1:c.-75-107701T>C	XP_016863883.1:n.-75-107701T>C
XR_001741482.1:n.600+145A>G
XR_001741483.1:n.600+145A>G
XR_001741484.1:n.600+145A>G
XR_001741485.1:n.600+145A>G
XR_001741486.1:n.506+145A>G