Canonical Allele Identifier: CA1985127089

Gene: TENM4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.79366149A>C , CM000673.2:g.79366149A>C	GRCh38
NC_000011.9:g.79077193A>C , CM000673.1:g.79077193A>C	GRCh37
NC_000011.8:g.78754841A>C	NCBI36
NG_051803.1:g.79503T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278550.12:c.-320-68606T>G MANE Select	ENSP00000278550.7:n.-320-68606T>G
ENST00000278550.11:c.-320-68606T>G	ENSP00000278550.7:n.-320-68606T>G
ENST00000528688.5:n.240-68606T>G
ENST00000531583.1:n.441-68606T>G
NM_001098816.2:c.-320-68606T>G	NP_001092286.2:n.-320-68606T>G
XM_011544924.1:c.-148-68606T>G	XP_011543226.1:n.-148-68606T>G
XM_011544925.1:c.-292-68606T>G	XP_011543227.1:n.-292-68606T>G
XM_011544927.1:c.-148-68606T>G	XP_011543229.1:n.-148-68606T>G
XM_011544928.1:c.-320-68606T>G	XP_011543230.1:n.-320-68606T>G
XM_011544929.1:c.-148-68606T>G	XP_011543231.1:n.-148-68606T>G
XM_011544930.1:c.-660-68606T>G	XP_011543232.1:n.-660-68606T>G
XM_017017525.1:c.-148-68606T>G	XP_016873014.1:n.-148-68606T>G
NM_001098816.3:c.-320-68606T>G MANE Select	NP_001092286.2:n.-320-68606T>G