Canonical Allele Identifier: CA367241698

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438050T>G (hg19) ; chr7:g.29398434T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398434T>G , CM000669.2:g.29398434T>G	GRCh38
NC_000007.13:g.29438050T>G , CM000669.1:g.29438050T>G	GRCh37
NC_000007.12:g.29404575T>G	NCBI36
NG_029365.2:g.256888T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.277T>G	ENSP00000386968.2:p.Tyr93Asp
ENST00000439384.6:n.500T>G
ENST00000446446.6:c.238T>G	ENSP00000396867.2:p.Tyr80Asp
ENST00000706158.1:c.*182T>G	ENSP00000516236.1:n.*182T>G
ENST00000706159.1:c.150T>G	ENSP00000516237.1:p.Pro50=
ENST00000706160.1:c.238T>G	ENSP00000516238.1:p.Tyr80Asp
ENST00000706161.1:c.316T>G	ENSP00000516239.1:p.Tyr106Asp
ENST00000706162.1:c.238T>G	ENSP00000516240.1:p.Tyr80Asp
ENST00000706163.1:c.50-81845T>G	ENSP00000516241.1:n.50-81845T>G
ENST00000222792.11:c.238T>G MANE Select	ENSP00000222792.7:p.Tyr80Asp
ENST00000644824.1:c.463T>G	ENSP00000495614.1:p.Tyr155Asp
ENST00000222792.10:c.238T>G	ENSP00000222792.6:p.Tyr80Asp
ENST00000409350.5:c.277T>G	ENSP00000386968.1:p.Tyr93Asp
ENST00000409922.5:n.449T>G
ENST00000409964.6:n.437T>G
ENST00000412536.5:n.258T>G
ENST00000435288.6:c.168+4732T>G	ENSP00000400282.3:n.168+4732T>G
ENST00000439384.5:c.463T>G	ENSP00000409843.1:p.Tyr155Asp
ENST00000474070.5:c.338T>G
ENST00000478128.6:n.332T>G
ENST00000482820.6:n.447T>G
ENST00000491856.1:n.1787T>G
ENST00000495789.6:c.238T>G	ENSP00000438587.2:p.Tyr80Asp
ENST00000539389.5:c.238T>G	ENSP00000440526.2:p.Tyr80Asp
ENST00000539406.5:c.238T>G	ENSP00000444063.2:p.Tyr80Asp
NM_001293069.1:c.463T>G	NP_001279998.1:p.Tyr155Asp
NM_001293070.1:c.277T>G	NP_001279999.1:p.Tyr93Asp
NM_001293071.1:c.133T>G	NP_001280000.1:p.Tyr45Asp
NM_001293072.1:c.193T>G	NP_001280001.1:p.Tyr65Asp
NM_004067.3:c.238T>G	NP_004058.1:p.Tyr80Asp
XM_011515105.1:c.541T>G	XP_011513407.1:p.Tyr181Asp
XM_011515106.1:c.502T>G	XP_011513408.1:p.Tyr168Asp
XM_011515107.1:c.316T>G	XP_011513409.1:p.Tyr106Asp
XM_011515108.1:c.238T>G	XP_011513410.1:p.Tyr80Asp
XM_011515109.1:c.199T>G	XP_011513411.1:p.Tyr67Asp
XM_011515110.1:c.160T>G	XP_011513412.1:p.Tyr54Asp
XM_011515111.1:c.133T>G	XP_011513413.1:p.Tyr45Asp
XM_011515112.1:c.541T>G	XP_011513414.1:p.Tyr181Asp
XM_011515105.2:c.541T>G	XP_011513407.1:p.Tyr181Asp
XM_011515106.2:c.502T>G	XP_011513408.1:p.Tyr168Asp
XM_011515107.2:c.316T>G	XP_011513409.1:p.Tyr106Asp
XM_017011721.1:c.559T>G	XP_016867210.1:p.Tyr187Asp
XM_017011722.1:c.334T>G	XP_016867211.1:p.Tyr112Asp
NM_004067.4:c.238T>G MANE Select	NP_004058.1:p.Tyr80Asp
NM_001293070.2:c.277T>G	NP_001279999.1:p.Tyr93Asp
NM_001293071.2:c.133T>G	NP_001280000.1:p.Tyr45Asp
NM_001293072.2:c.193T>G	NP_001280001.1:p.Tyr65Asp
NM_001398427.1:c.-201T>G	NP_001385356.1:n.-201T>G