Canonical Allele Identifier: CA349049785

Gene: TTC21B

Linked Data

• gnomAD v4: 2-165898741-T-G
• MyVariant Identifiers: chr2:g.166755251T>G (hg19) ; chr2:g.165898741T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.165898741T>G , CM000664.2:g.165898741T>G	GRCh38
NC_000002.11:g.166755251T>G , CM000664.1:g.166755251T>G	GRCh37
NC_000002.10:g.166463497T>G	NCBI36
NG_030345.1:g.60098A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243344.8:c.2895A>C MANE Select	ENSP00000243344.7:p.Lys965Asn
ENST00000652557.1:c.2895A>C	ENSP00000498617.1:p.Lys965Asn
ENST00000679356.1:c.2895A>C	ENSP00000506245.1:p.Lys965Asn
ENST00000679676.1:c.2784A>C	ENSP00000505492.1:p.Lys928Asn
ENST00000679799.1:c.2895A>C	ENSP00000505208.1:p.Lys965Asn
ENST00000679840.1:c.2895A>C	ENSP00000505248.1:p.Lys965Asn
ENST00000679931.1:c.*1937A>C	ENSP00000505632.1:n.*1937A>C
ENST00000679967.1:c.2895A>C	ENSP00000506607.1:p.Lys965Asn
ENST00000680327.1:c.*1937A>C	ENSP00000506639.1:n.*1937A>C
ENST00000680448.1:c.2895A>C	ENSP00000505921.1:p.Lys965Asn
ENST00000680657.1:n.3006A>C
ENST00000680690.1:c.*2147A>C	ENSP00000506121.1:n.*2147A>C
ENST00000680888.1:c.2895A>C	ENSP00000506276.1:p.Lys965Asn
ENST00000680925.1:n.925A>C
ENST00000680947.1:c.*2167A>C	ENSP00000506496.1:n.*2167A>C
ENST00000681024.1:c.2895A>C	ENSP00000506449.1:p.Lys965Asn
ENST00000681083.1:c.*2629A>C	ENSP00000506095.1:n.*2629A>C
ENST00000681167.1:n.2769A>C
ENST00000681483.1:c.2895A>C	ENSP00000505499.1:p.Lys965Asn
ENST00000681502.1:c.*2319A>C	ENSP00000505644.1:n.*2319A>C
ENST00000681606.1:c.2895A>C	ENSP00000505354.1:p.Lys965Asn
ENST00000681819.1:c.2895A>C	ENSP00000505673.1:p.Lys965Asn
ENST00000681952.1:c.2895A>C	ENSP00000506400.1:p.Lys965Asn
ENST00000243344.7:c.2895A>C	ENSP00000243344.7:p.Lys965Asn
ENST00000484129.1:n.370A>C
NM_024753.4:c.2895A>C	NP_079029.3:p.Lys965Asn
XM_006712761.1:c.2895A>C	XP_006712824.1:p.Lys965Asn
XM_011511870.1:c.2328A>C	XP_011510172.1:p.Lys776Asn
XM_011511871.1:c.2145A>C	XP_011510173.1:p.Lys715Asn
XM_011511872.1:c.*97A>C	XP_011510174.1:n.*97A>C
XM_011511871.3:c.2145A>C	XP_011510173.1:p.Lys715Asn
XM_011511872.2:c.*97A>C	XP_011510174.1:n.*97A>C
XM_017004967.1:c.2895A>C	XP_016860456.1:p.Lys965Asn
XM_017004968.2:c.2241A>C	XP_016860457.1:p.Lys747Asn
XM_017004969.1:c.1896A>C	XP_016860458.1:p.Lys632Asn
NM_024753.5:c.2895A>C MANE Select	NP_079029.3:p.Lys965Asn