Canonical Allele Identifier: CA1697231126

Gene: CHN2

Linked Data

• dbSNP Id: rs1801899309

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398061_29398062insCG , CM000669.2:g.29398061_29398062insCG	GRCh38
NC_000007.13:g.29437677_29437678insCG , CM000669.1:g.29437677_29437678insCG	GRCh37
NC_000007.12:g.29404202_29404203insCG	NCBI36
NG_029365.2:g.256515_256516insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.216-312_216-311insCG	ENSP00000386968.2:n.216-312_216-311insCG
ENST00000439384.6:n.439-312_439-311insCG
ENST00000446446.6:c.177-312_177-311insCG	ENSP00000396867.2:n.177-312_177-311insCG
ENST00000706158.1:c.*121-312_*121-311insCG	ENSP00000516236.1:n.*121-312_*121-311insCG
ENST00000706159.1:c.89-312_89-311insCG	ENSP00000516237.1:n.89-312_89-311insCG
ENST00000706160.1:c.177-312_177-311insCG	ENSP00000516238.1:n.177-312_177-311insCG
ENST00000706161.1:c.255-312_255-311insCG	ENSP00000516239.1:n.255-312_255-311insCG
ENST00000706162.1:c.177-312_177-311insCG	ENSP00000516240.1:n.177-312_177-311insCG
ENST00000706163.1:c.50-82218_50-82217insCG	ENSP00000516241.1:n.50-82218_50-82217insCG
ENST00000222792.11:c.177-312_177-311insCG MANE Select	ENSP00000222792.7:n.177-312_177-311insCG
ENST00000644824.1:c.402-312_402-311insCG	ENSP00000495614.1:n.402-312_402-311insCG
ENST00000222792.10:c.177-312_177-311insCG	ENSP00000222792.6:n.177-312_177-311insCG
ENST00000409350.5:c.216-312_216-311insCG	ENSP00000386968.1:n.216-312_216-311insCG
ENST00000409922.5:n.388-312_388-311insCG
ENST00000409964.6:n.376-312_376-311insCG
ENST00000412536.5:n.197-312_197-311insCG
ENST00000435288.6:c.168+4359_168+4360insCG	ENSP00000400282.3:n.168+4359_168+4360insCG
ENST00000439384.5:c.402-312_402-311insCG	ENSP00000409843.1:n.402-312_402-311insCG
ENST00000474070.5:c.277-312_277-311insCG
ENST00000478128.6:n.271-312_271-311insCG
ENST00000482820.6:n.386-312_386-311insCG
ENST00000491856.1:n.1414_1415insCG
ENST00000495789.6:c.177-312_177-311insCG	ENSP00000438587.2:n.177-312_177-311insCG
ENST00000539389.5:c.177-312_177-311insCG	ENSP00000440526.2:n.177-312_177-311insCG
ENST00000539406.5:c.177-312_177-311insCG	ENSP00000444063.2:n.177-312_177-311insCG
NM_001293069.1:c.402-312_402-311insCG	NP_001279998.1:n.402-312_402-311insCG
NM_001293070.1:c.216-312_216-311insCG	NP_001279999.1:n.216-312_216-311insCG
NM_001293071.1:c.72-312_72-311insCG	NP_001280000.1:n.72-312_72-311insCG
NM_001293072.1:c.132-312_132-311insCG	NP_001280001.1:n.132-312_132-311insCG
NM_004067.3:c.177-312_177-311insCG	NP_004058.1:n.177-312_177-311insCG
XM_011515105.1:c.480-312_480-311insCG	XP_011513407.1:n.480-312_480-311insCG
XM_011515106.1:c.441-312_441-311insCG	XP_011513408.1:n.441-312_441-311insCG
XM_011515107.1:c.255-312_255-311insCG	XP_011513409.1:n.255-312_255-311insCG
XM_011515108.1:c.177-312_177-311insCG	XP_011513410.1:n.177-312_177-311insCG
XM_011515109.1:c.138-312_138-311insCG	XP_011513411.1:n.138-312_138-311insCG
XM_011515110.1:c.99-312_99-311insCG	XP_011513412.1:n.99-312_99-311insCG
XM_011515111.1:c.72-312_72-311insCG	XP_011513413.1:n.72-312_72-311insCG
XM_011515112.1:c.480-312_480-311insCG	XP_011513414.1:n.480-312_480-311insCG
XM_011515105.2:c.480-312_480-311insCG	XP_011513407.1:n.480-312_480-311insCG
XM_011515106.2:c.441-312_441-311insCG	XP_011513408.1:n.441-312_441-311insCG
XM_011515107.2:c.255-312_255-311insCG	XP_011513409.1:n.255-312_255-311insCG
XM_017011721.1:c.498-312_498-311insCG	XP_016867210.1:n.498-312_498-311insCG
XM_017011722.1:c.273-312_273-311insCG	XP_016867211.1:n.273-312_273-311insCG
NM_004067.4:c.177-312_177-311insCG MANE Select	NP_004058.1:n.177-312_177-311insCG
NM_001293070.2:c.216-312_216-311insCG	NP_001279999.1:n.216-312_216-311insCG
NM_001293071.2:c.72-312_72-311insCG	NP_001280000.1:n.72-312_72-311insCG
NM_001293072.2:c.132-312_132-311insCG	NP_001280001.1:n.132-312_132-311insCG
NM_001398427.1:c.-262-312_-262-311insCG	NP_001385356.1:n.-262-312_-262-311insCG