Canonical Allele Identifier: CA1697231327
Gene: CHN2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000409350.6:c.277T= ENSP00000386968.2:p.Tyr93=
ENST00000439384.6:n.500T=
ENST00000446446.6:c.238T= ENSP00000396867.2:p.Tyr80=
ENST00000706158.1:c.*182T= ENSP00000516236.1:n.*182T=
ENST00000706159.1:c.150T= ENSP00000516237.1:p.Pro50=
ENST00000706160.1:c.238T= ENSP00000516238.1:p.Tyr80=
ENST00000706161.1:c.316T= ENSP00000516239.1:p.Tyr106=
ENST00000706162.1:c.238T= ENSP00000516240.1:p.Tyr80=
ENST00000706163.1:c.50-81845T= ENSP00000516241.1:n.50-81845T=
ENST00000222792.11:c.238T= MANE Select ENSP00000222792.7:p.Tyr80=
ENST00000644824.1:c.463T= ENSP00000495614.1:p.Tyr155=
ENST00000222792.10:c.238T= ENSP00000222792.6:p.Tyr80=
ENST00000409350.5:c.277T= ENSP00000386968.1:p.Tyr93=
ENST00000409922.5:n.449T=
ENST00000409964.6:n.437T=
ENST00000412536.5:n.258T=
ENST00000435288.6:c.168+4732T= ENSP00000400282.3:n.168+4732T=
ENST00000439384.5:c.463T= ENSP00000409843.1:p.Tyr155=
ENST00000474070.5:c.338T=
ENST00000478128.6:n.332T=
ENST00000482820.6:n.447T=
ENST00000491856.1:n.1787T=
ENST00000495789.6:c.238T= ENSP00000438587.2:p.Tyr80=
ENST00000539389.5:c.238T= ENSP00000440526.2:p.Tyr80=
ENST00000539406.5:c.238T= ENSP00000444063.2:p.Tyr80=
NM_001293069.1:c.463T= NP_001279998.1:p.Tyr155=
NM_001293070.1:c.277T= NP_001279999.1:p.Tyr93=
NM_001293071.1:c.133T= NP_001280000.1:p.Tyr45=
NM_001293072.1:c.193T= NP_001280001.1:p.Tyr65=
NM_004067.3:c.238T= NP_004058.1:p.Tyr80=
XM_011515105.1:c.541T= XP_011513407.1:p.Tyr181=
XM_011515106.1:c.502T= XP_011513408.1:p.Tyr168=
XM_011515107.1:c.316T= XP_011513409.1:p.Tyr106=
XM_011515108.1:c.238T= XP_011513410.1:p.Tyr80=
XM_011515109.1:c.199T= XP_011513411.1:p.Tyr67=
XM_011515110.1:c.160T= XP_011513412.1:p.Tyr54=
XM_011515111.1:c.133T= XP_011513413.1:p.Tyr45=
XM_011515112.1:c.541T= XP_011513414.1:p.Tyr181=
XM_011515105.2:c.541T= XP_011513407.1:p.Tyr181=
XM_011515106.2:c.502T= XP_011513408.1:p.Tyr168=
XM_011515107.2:c.316T= XP_011513409.1:p.Tyr106=
XM_017011721.1:c.559T= XP_016867210.1:p.Tyr187=
XM_017011722.1:c.334T= XP_016867211.1:p.Tyr112=
NM_004067.4:c.238T= MANE Select NP_004058.1:p.Tyr80=
NM_001293070.2:c.277T= NP_001279999.1:p.Tyr93=
NM_001293071.2:c.133T= NP_001280000.1:p.Tyr45=
NM_001293072.2:c.193T= NP_001280001.1:p.Tyr65=
NM_001398427.1:c.-201T= NP_001385356.1:n.-201T=