Canonical Allele Identifier: CA387137341

Gene: TCTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.123688050G>C , CM000674.2:g.123688050G>C	GRCh38
NC_000012.11:g.124172597G>C , CM000674.1:g.124172597G>C	GRCh37
NC_000012.10:g.122738550G>C	NCBI36
NG_030442.1:g.21938G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024809.5:c.765-1G>C MANE Select	NP_079085.2:n.765-1G>C
ENST00000303372.7:c.765-1G>C MANE Select	ENSP00000304941.5:n.765-1G>C
NM_001143850.2:c.762-1G>C	NP_001137322.1:n.762-1G>C
NM_001143850.3:c.762-1G>C	NP_001137322.1:n.762-1G>C
NM_024809.4:c.765-1G>C	NP_079085.2:n.765-1G>C
ENST00000303372.6:c.765-1G>C	ENSP00000304941.5:n.765-1G>C
ENST00000426174.6:c.762-1G>C	ENSP00000395171.2:n.762-1G>C
ENST00000679504.1:c.762-1G>C	ENSP00000505006.1:n.762-1G>C
ENST00000680500.1:c.765-1G>C	ENSP00000506438.1:n.765-1G>C
ENST00000680574.1:c.765-1G>C	ENSP00000505356.1:n.765-1G>C
XM_005253623.2:c.765-1G>C	XP_005253680.1:n.765-1G>C
XM_006719605.2:c.765-1G>C	XP_006719668.1:n.765-1G>C
XM_006719605.3:c.765-1G>C	XP_006719668.1:n.765-1G>C
XM_011538748.1:c.-22+1015G>C	XP_011537050.1:n.-22+1015G>C
XM_017019974.1:c.762-1G>C	XP_016875463.1:n.762-1G>C
XM_017019975.1:c.-22+1015G>C	XP_016875464.1:n.-22+1015G>C