Canonical Allele Identifier: CA1697231408

Gene: CHN2

Linked Data

• dbSNP Id: rs1801955498
• gnomAD v4: 7-29398616-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398616_29398617insT , CM000669.2:g.29398616_29398617insT	GRCh38
NC_000007.13:g.29438232_29438233insT , CM000669.1:g.29438232_29438233insT	GRCh37
NC_000007.12:g.29404757_29404758insT	NCBI36
NG_029365.2:g.257070_257071insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.329+130_329+131insT	ENSP00000386968.2:n.329+130_329+131insT
ENST00000439384.6:n.552+130_552+131insT
ENST00000446446.6:c.290+130_290+131insT	ENSP00000396867.2:n.290+130_290+131insT
ENST00000706158.1:c.*234+130_*234+131insT	ENSP00000516236.1:n.*234+130_*234+131insT
ENST00000706159.1:c.202+130_202+131insT	ENSP00000516237.1:n.202+130_202+131insT
ENST00000706160.1:c.290+130_290+131insT	ENSP00000516238.1:n.290+130_290+131insT
ENST00000706161.1:c.368+130_368+131insT	ENSP00000516239.1:n.368+130_368+131insT
ENST00000706162.1:c.290+130_290+131insT	ENSP00000516240.1:n.290+130_290+131insT
ENST00000706163.1:c.50-81663_50-81662insT	ENSP00000516241.1:n.50-81663_50-81662insT
ENST00000222792.11:c.290+130_290+131insT MANE Select	ENSP00000222792.7:n.290+130_290+131insT
ENST00000644824.1:c.515+130_515+131insT	ENSP00000495614.1:n.515+130_515+131insT
ENST00000222792.10:c.290+130_290+131insT	ENSP00000222792.6:n.290+130_290+131insT
ENST00000409350.5:c.329+130_329+131insT	ENSP00000386968.1:n.329+130_329+131insT
ENST00000409922.5:n.501+130_501+131insT
ENST00000409964.6:n.489+130_489+131insT
ENST00000412536.5:n.310+130_310+131insT
ENST00000435288.6:c.168+4914_168+4915insT	ENSP00000400282.3:n.168+4914_168+4915insT
ENST00000439384.5:c.515+130_515+131insT	ENSP00000409843.1:n.515+130_515+131insT
ENST00000474070.5:c.390+130_390+131insT
ENST00000478128.6:n.384+130_384+131insT
ENST00000491856.1:n.1839+130_1839+131insT
ENST00000495789.6:c.290+130_290+131insT	ENSP00000438587.2:n.290+130_290+131insT
ENST00000539389.5:c.290+130_290+131insT	ENSP00000440526.2:n.290+130_290+131insT
ENST00000539406.5:c.290+130_290+131insT	ENSP00000444063.2:n.290+130_290+131insT
NM_001293069.1:c.515+130_515+131insT	NP_001279998.1:n.515+130_515+131insT
NM_001293070.1:c.329+130_329+131insT	NP_001279999.1:n.329+130_329+131insT
NM_001293071.1:c.185+130_185+131insT	NP_001280000.1:n.185+130_185+131insT
NM_001293072.1:c.245+130_245+131insT	NP_001280001.1:n.245+130_245+131insT
NM_004067.3:c.290+130_290+131insT	NP_004058.1:n.290+130_290+131insT
XM_011515105.1:c.593+130_593+131insT	XP_011513407.1:n.593+130_593+131insT
XM_011515106.1:c.554+130_554+131insT	XP_011513408.1:n.554+130_554+131insT
XM_011515107.1:c.368+130_368+131insT	XP_011513409.1:n.368+130_368+131insT
XM_011515108.1:c.290+130_290+131insT	XP_011513410.1:n.290+130_290+131insT
XM_011515109.1:c.251+130_251+131insT	XP_011513411.1:n.251+130_251+131insT
XM_011515110.1:c.212+130_212+131insT	XP_011513412.1:n.212+130_212+131insT
XM_011515111.1:c.185+130_185+131insT	XP_011513413.1:n.185+130_185+131insT
XM_011515112.1:c.593+130_593+131insT	XP_011513414.1:n.593+130_593+131insT
XM_011515105.2:c.593+130_593+131insT	XP_011513407.1:n.593+130_593+131insT
XM_011515106.2:c.554+130_554+131insT	XP_011513408.1:n.554+130_554+131insT
XM_011515107.2:c.368+130_368+131insT	XP_011513409.1:n.368+130_368+131insT
XM_017011721.1:c.611+130_611+131insT	XP_016867210.1:n.611+130_611+131insT
XM_017011722.1:c.386+130_386+131insT	XP_016867211.1:n.386+130_386+131insT
NM_004067.4:c.290+130_290+131insT MANE Select	NP_004058.1:n.290+130_290+131insT
NM_001293070.2:c.329+130_329+131insT	NP_001279999.1:n.329+130_329+131insT
NM_001293071.2:c.185+130_185+131insT	NP_001280000.1:n.185+130_185+131insT
NM_001293072.2:c.245+130_245+131insT	NP_001280001.1:n.245+130_245+131insT
NM_001398427.1:c.-149+130_-149+131insT	NP_001385356.1:n.-149+130_-149+131insT