Canonical Allele Identifier: CA349051976

Gene: TTC21B TTC21B-AS1

Linked Data

• MyVariant Identifiers: chr2:g.166799770C>G (hg19) ; chr2:g.165943260C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165943260C>G , CM000664.2:g.165943260C>G	GRCh38
NC_000002.11:g.166799770C>G , CM000664.1:g.166799770C>G	GRCh37
NC_000002.10:g.166508016C>G	NCBI36
NG_030345.1:g.15579G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.511G>C (TTC21B) MANE Select	ENSP00000243344.7:p.Gly171Arg
ENST00000652557.1:c.511G>C (TTC21B)	ENSP00000498617.1:p.Gly171Arg
ENST00000679356.1:c.511G>C (TTC21B)	ENSP00000506245.1:p.Gly171Arg
ENST00000679671.1:n.624G>C (TTC21B)
ENST00000679676.1:c.400G>C (TTC21B)	ENSP00000505492.1:p.Gly134Arg
ENST00000679799.1:c.511G>C (TTC21B)	ENSP00000505208.1:p.Gly171Arg
ENST00000679840.1:c.511G>C (TTC21B)	ENSP00000505248.1:p.Gly171Arg
ENST00000679931.1:c.511G>C (TTC21B)	ENSP00000505632.1:p.Gly171Arg
ENST00000679967.1:c.511G>C (TTC21B)	ENSP00000506607.1:p.Gly171Arg
ENST00000680327.1:c.511G>C (TTC21B)	ENSP00000506639.1:p.Gly171Arg
ENST00000680448.1:c.511G>C (TTC21B)	ENSP00000505921.1:p.Gly171Arg
ENST00000680657.1:n.622G>C (TTC21B)
ENST00000680690.1:c.511G>C (TTC21B)	ENSP00000506121.1:p.Gly171Arg
ENST00000680888.1:c.511G>C (TTC21B)	ENSP00000506276.1:p.Gly171Arg
ENST00000680947.1:c.511G>C (TTC21B)	ENSP00000506496.1:p.Gly171Arg
ENST00000681024.1:c.511G>C (TTC21B)	ENSP00000506449.1:p.Gly171Arg
ENST00000681083.1:c.*245G>C (TTC21B)	ENSP00000506095.1:n.*245G>C
ENST00000681483.1:c.511G>C (TTC21B)	ENSP00000505499.1:p.Gly171Arg
ENST00000681502.1:c.511G>C (TTC21B)	ENSP00000505644.1:p.Gly171Arg
ENST00000681606.1:c.511G>C (TTC21B)	ENSP00000505354.1:p.Gly171Arg
ENST00000681819.1:c.511G>C (TTC21B)	ENSP00000505673.1:p.Gly171Arg
ENST00000681952.1:c.511G>C (TTC21B)	ENSP00000506400.1:p.Gly171Arg
ENST00000243344.7:c.511G>C (TTC21B)	ENSP00000243344.7:p.Gly171Arg
ENST00000464374.5:n.551G>C (TTC21B)
NM_024753.4:c.511G>C (TTC21B)	NP_079029.3:p.Gly171Arg
NR_038983.1:n.277-3937C>G (TTC21B-AS1)
NR_038984.1:n.221-3937C>G (TTC21B-AS1)
XM_006712761.1:c.511G>C (TTC21B)	XP_006712824.1:p.Gly171Arg
XM_011511870.1:c.-57G>C (TTC21B)	XP_011510172.1:n.-57G>C
XM_011511872.1:c.511G>C (TTC21B)	XP_011510174.1:p.Gly171Arg
XM_011511872.2:c.511G>C (TTC21B)	XP_011510174.1:p.Gly171Arg
XM_017004967.1:c.511G>C (TTC21B)	XP_016860456.1:p.Gly171Arg
XM_017004969.1:c.-506G>C (TTC21B)	XP_016860458.1:n.-506G>C
NM_024753.5:c.511G>C (TTC21B) MANE Select	NP_079029.3:p.Gly171Arg