Canonical Allele Identifier: CA1697231302
Gene: CHN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.29398366C= , CM000669.2:g.29398366C= GRCh38
NC_000007.13:g.29437982C= , CM000669.1:g.29437982C= GRCh37
NC_000007.12:g.29404507C= NCBI36
NG_029365.2:g.256820C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000409350.6:c.216-7C= ENSP00000386968.2:n.216-7C=
ENST00000439384.6:n.439-7C=
ENST00000446446.6:c.177-7C= ENSP00000396867.2:n.177-7C=
ENST00000706158.1:c.*121-7C= ENSP00000516236.1:n.*121-7C=
ENST00000706159.1:c.89-7C= ENSP00000516237.1:n.89-7C=
ENST00000706160.1:c.177-7C= ENSP00000516238.1:n.177-7C=
ENST00000706161.1:c.255-7C= ENSP00000516239.1:n.255-7C=
ENST00000706162.1:c.177-7C= ENSP00000516240.1:n.177-7C=
ENST00000706163.1:c.50-81913C= ENSP00000516241.1:n.50-81913C=
ENST00000222792.11:c.177-7C= MANE Select ENSP00000222792.7:n.177-7C=
ENST00000644824.1:c.402-7C= ENSP00000495614.1:n.402-7C=
ENST00000222792.10:c.177-7C= ENSP00000222792.6:n.177-7C=
ENST00000409350.5:c.216-7C= ENSP00000386968.1:n.216-7C=
ENST00000409922.5:n.388-7C=
ENST00000409964.6:n.376-7C=
ENST00000412536.5:n.197-7C=
ENST00000435288.6:c.168+4664C= ENSP00000400282.3:n.168+4664C=
ENST00000439384.5:c.402-7C= ENSP00000409843.1:n.402-7C=
ENST00000474070.5:c.277-7C=
ENST00000478128.6:n.271-7C=
ENST00000482820.6:n.386-7C=
ENST00000491856.1:n.1719C=
ENST00000495789.6:c.177-7C= ENSP00000438587.2:n.177-7C=
ENST00000539389.5:c.177-7C= ENSP00000440526.2:n.177-7C=
ENST00000539406.5:c.177-7C= ENSP00000444063.2:n.177-7C=
NM_001293069.1:c.402-7C= NP_001279998.1:n.402-7C=
NM_001293070.1:c.216-7C= NP_001279999.1:n.216-7C=
NM_001293071.1:c.72-7C= NP_001280000.1:n.72-7C=
NM_001293072.1:c.132-7C= NP_001280001.1:n.132-7C=
NM_004067.3:c.177-7C= NP_004058.1:n.177-7C=
XM_011515105.1:c.480-7C= XP_011513407.1:n.480-7C=
XM_011515106.1:c.441-7C= XP_011513408.1:n.441-7C=
XM_011515107.1:c.255-7C= XP_011513409.1:n.255-7C=
XM_011515108.1:c.177-7C= XP_011513410.1:n.177-7C=
XM_011515109.1:c.138-7C= XP_011513411.1:n.138-7C=
XM_011515110.1:c.99-7C= XP_011513412.1:n.99-7C=
XM_011515111.1:c.72-7C= XP_011513413.1:n.72-7C=
XM_011515112.1:c.480-7C= XP_011513414.1:n.480-7C=
XM_011515105.2:c.480-7C= XP_011513407.1:n.480-7C=
XM_011515106.2:c.441-7C= XP_011513408.1:n.441-7C=
XM_011515107.2:c.255-7C= XP_011513409.1:n.255-7C=
XM_017011721.1:c.498-7C= XP_016867210.1:n.498-7C=
XM_017011722.1:c.273-7C= XP_016867211.1:n.273-7C=
NM_004067.4:c.177-7C= MANE Select NP_004058.1:n.177-7C=
NM_001293070.2:c.216-7C= NP_001279999.1:n.216-7C=
NM_001293071.2:c.72-7C= NP_001280000.1:n.72-7C=
NM_001293072.2:c.132-7C= NP_001280001.1:n.132-7C=
NM_001398427.1:c.-262-7C= NP_001385356.1:n.-262-7C=