Canonical Allele Identifier: CA2774871224

Gene: CHN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398068_29398069insCT , CM000669.2:g.29398068_29398069insCT	GRCh38
NC_000007.13:g.29437684_29437685insCT , CM000669.1:g.29437684_29437685insCT	GRCh37
NC_000007.12:g.29404209_29404210insCT	NCBI36
NG_029365.2:g.256522_256523insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.216-305_216-304insCT	ENSP00000386968.2:n.216-305_216-304insCT
ENST00000439384.6:n.439-305_439-304insCT
ENST00000446446.6:c.177-305_177-304insCT	ENSP00000396867.2:n.177-305_177-304insCT
ENST00000706158.1:c.*121-305_*121-304insCT	ENSP00000516236.1:n.*121-305_*121-304insCT
ENST00000706159.1:c.89-305_89-304insCT	ENSP00000516237.1:n.89-305_89-304insCT
ENST00000706160.1:c.177-305_177-304insCT	ENSP00000516238.1:n.177-305_177-304insCT
ENST00000706161.1:c.255-305_255-304insCT	ENSP00000516239.1:n.255-305_255-304insCT
ENST00000706162.1:c.177-305_177-304insCT	ENSP00000516240.1:n.177-305_177-304insCT
ENST00000706163.1:c.50-82211_50-82210insCT	ENSP00000516241.1:n.50-82211_50-82210insCT
ENST00000222792.11:c.177-305_177-304insCT MANE Select	ENSP00000222792.7:n.177-305_177-304insCT
ENST00000644824.1:c.402-305_402-304insCT	ENSP00000495614.1:n.402-305_402-304insCT
ENST00000222792.10:c.177-305_177-304insCT	ENSP00000222792.6:n.177-305_177-304insCT
ENST00000409350.5:c.216-305_216-304insCT	ENSP00000386968.1:n.216-305_216-304insCT
ENST00000409922.5:n.388-305_388-304insCT
ENST00000409964.6:n.376-305_376-304insCT
ENST00000412536.5:n.197-305_197-304insCT
ENST00000435288.6:c.168+4366_168+4367insCT	ENSP00000400282.3:n.168+4366_168+4367insCT
ENST00000439384.5:c.402-305_402-304insCT	ENSP00000409843.1:n.402-305_402-304insCT
ENST00000474070.5:c.277-305_277-304insCT
ENST00000478128.6:n.271-305_271-304insCT
ENST00000482820.6:n.386-305_386-304insCT
ENST00000491856.1:n.1421_1422insCT
ENST00000495789.6:c.177-305_177-304insCT	ENSP00000438587.2:n.177-305_177-304insCT
ENST00000539389.5:c.177-305_177-304insCT	ENSP00000440526.2:n.177-305_177-304insCT
ENST00000539406.5:c.177-305_177-304insCT	ENSP00000444063.2:n.177-305_177-304insCT
NM_001293069.1:c.402-305_402-304insCT	NP_001279998.1:n.402-305_402-304insCT
NM_001293070.1:c.216-305_216-304insCT	NP_001279999.1:n.216-305_216-304insCT
NM_001293071.1:c.72-305_72-304insCT	NP_001280000.1:n.72-305_72-304insCT
NM_001293072.1:c.132-305_132-304insCT	NP_001280001.1:n.132-305_132-304insCT
NM_004067.3:c.177-305_177-304insCT	NP_004058.1:n.177-305_177-304insCT
XM_011515105.1:c.480-305_480-304insCT	XP_011513407.1:n.480-305_480-304insCT
XM_011515106.1:c.441-305_441-304insCT	XP_011513408.1:n.441-305_441-304insCT
XM_011515107.1:c.255-305_255-304insCT	XP_011513409.1:n.255-305_255-304insCT
XM_011515108.1:c.177-305_177-304insCT	XP_011513410.1:n.177-305_177-304insCT
XM_011515109.1:c.138-305_138-304insCT	XP_011513411.1:n.138-305_138-304insCT
XM_011515110.1:c.99-305_99-304insCT	XP_011513412.1:n.99-305_99-304insCT
XM_011515111.1:c.72-305_72-304insCT	XP_011513413.1:n.72-305_72-304insCT
XM_011515112.1:c.480-305_480-304insCT	XP_011513414.1:n.480-305_480-304insCT
XM_011515105.2:c.480-305_480-304insCT	XP_011513407.1:n.480-305_480-304insCT
XM_011515106.2:c.441-305_441-304insCT	XP_011513408.1:n.441-305_441-304insCT
XM_011515107.2:c.255-305_255-304insCT	XP_011513409.1:n.255-305_255-304insCT
XM_017011721.1:c.498-305_498-304insCT	XP_016867210.1:n.498-305_498-304insCT
XM_017011722.1:c.273-305_273-304insCT	XP_016867211.1:n.273-305_273-304insCT
NM_004067.4:c.177-305_177-304insCT MANE Select	NP_004058.1:n.177-305_177-304insCT
NM_001293070.2:c.216-305_216-304insCT	NP_001279999.1:n.216-305_216-304insCT
NM_001293071.2:c.72-305_72-304insCT	NP_001280000.1:n.72-305_72-304insCT
NM_001293072.2:c.132-305_132-304insCT	NP_001280001.1:n.132-305_132-304insCT
NM_001398427.1:c.-262-305_-262-304insCT	NP_001385356.1:n.-262-305_-262-304insCT