Canonical Allele Identifier: CA387161604

Gene: TCTN2

Linked Data

• MyVariant Identifiers: chr12:g.124171443G>C (hg19) ; chr12:g.123686896G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123686896G>C , CM000674.2:g.123686896G>C	GRCh38
NC_000012.11:g.124171443G>C , CM000674.1:g.124171443G>C	GRCh37
NC_000012.10:g.122737396G>C	NCBI36
NG_030442.1:g.20784G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000303372.7:c.625G>C MANE Select	ENSP00000304941.5:p.Gly209Arg
ENST00000679504.1:c.622G>C	ENSP00000505006.1:p.Gly208Arg
ENST00000680500.1:c.625G>C	ENSP00000506438.1:p.Gly209Arg
ENST00000680574.1:c.625G>C	ENSP00000505356.1:p.Gly209Arg
ENST00000303372.6:c.625G>C	ENSP00000304941.5:p.Gly209Arg
ENST00000426174.6:c.622G>C	ENSP00000395171.2:p.Gly208Arg
NM_001143850.2:c.622G>C	NP_001137322.1:p.Gly208Arg
NM_024809.4:c.625G>C	NP_079085.2:p.Gly209Arg
XM_005253623.2:c.625G>C	XP_005253680.1:p.Gly209Arg
XM_006719605.2:c.625G>C	XP_006719668.1:p.Gly209Arg
XM_006719605.3:c.625G>C	XP_006719668.1:p.Gly209Arg
XM_017019974.1:c.622G>C	XP_016875463.1:p.Gly208Arg
XM_017019975.1:c.-161G>C	XP_016875464.1:n.-161G>C
NM_024809.5:c.625G>C MANE Select	NP_079085.2:p.Gly209Arg
NM_001143850.3:c.622G>C	NP_001137322.1:p.Gly208Arg