Canonical Allele Identifier: CA367241569

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29437989G>C (hg19) ; chr7:g.29398373G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398373G>C , CM000669.2:g.29398373G>C	GRCh38
NC_000007.13:g.29437989G>C , CM000669.1:g.29437989G>C	GRCh37
NC_000007.12:g.29404514G>C	NCBI36
NG_029365.2:g.256827G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.216G>C	ENSP00000386968.2:p.Glu72Asp
ENST00000439384.6:n.439G>C
ENST00000446446.6:c.177G>C	ENSP00000396867.2:p.Glu59Asp
ENST00000706158.1:c.*121G>C	ENSP00000516236.1:n.*121G>C
ENST00000706159.1:c.89G>C	ENSP00000516237.1:p.Cys30Ser
ENST00000706160.1:c.177G>C	ENSP00000516238.1:p.Glu59Asp
ENST00000706161.1:c.255G>C	ENSP00000516239.1:p.Glu85Asp
ENST00000706162.1:c.177G>C	ENSP00000516240.1:p.Glu59Asp
ENST00000706163.1:c.50-81906G>C	ENSP00000516241.1:n.50-81906G>C
ENST00000222792.11:c.177G>C MANE Select	ENSP00000222792.7:p.Glu59Asp
ENST00000644824.1:c.402G>C	ENSP00000495614.1:p.Glu134Asp
ENST00000222792.10:c.177G>C	ENSP00000222792.6:p.Glu59Asp
ENST00000409350.5:c.216G>C	ENSP00000386968.1:p.Glu72Asp
ENST00000409922.5:n.388G>C
ENST00000409964.6:n.376G>C
ENST00000412536.5:n.197G>C
ENST00000435288.6:c.168+4671G>C	ENSP00000400282.3:n.168+4671G>C
ENST00000439384.5:c.402G>C	ENSP00000409843.1:p.Glu134Asp
ENST00000474070.5:c.277G>C
ENST00000478128.6:n.271G>C
ENST00000482820.6:n.386G>C
ENST00000491856.1:n.1726G>C
ENST00000495789.6:c.177G>C	ENSP00000438587.2:p.Glu59Asp
ENST00000539389.5:c.177G>C	ENSP00000440526.2:p.Glu59Asp
ENST00000539406.5:c.177G>C	ENSP00000444063.2:p.Glu59Asp
NM_001293069.1:c.402G>C	NP_001279998.1:p.Glu134Asp
NM_001293070.1:c.216G>C	NP_001279999.1:p.Glu72Asp
NM_001293071.1:c.72G>C	NP_001280000.1:p.Glu24Asp
NM_001293072.1:c.132G>C	NP_001280001.1:p.Glu44Asp
NM_004067.3:c.177G>C	NP_004058.1:p.Glu59Asp
XM_011515105.1:c.480G>C	XP_011513407.1:p.Glu160Asp
XM_011515106.1:c.441G>C	XP_011513408.1:p.Glu147Asp
XM_011515107.1:c.255G>C	XP_011513409.1:p.Glu85Asp
XM_011515108.1:c.177G>C	XP_011513410.1:p.Glu59Asp
XM_011515109.1:c.138G>C	XP_011513411.1:p.Glu46Asp
XM_011515110.1:c.99G>C	XP_011513412.1:p.Glu33Asp
XM_011515111.1:c.72G>C	XP_011513413.1:p.Glu24Asp
XM_011515112.1:c.480G>C	XP_011513414.1:p.Glu160Asp
XM_011515105.2:c.480G>C	XP_011513407.1:p.Glu160Asp
XM_011515106.2:c.441G>C	XP_011513408.1:p.Glu147Asp
XM_011515107.2:c.255G>C	XP_011513409.1:p.Glu85Asp
XM_017011721.1:c.498G>C	XP_016867210.1:p.Glu166Asp
XM_017011722.1:c.273G>C	XP_016867211.1:p.Glu91Asp
NM_004067.4:c.177G>C MANE Select	NP_004058.1:p.Glu59Asp
NM_001293070.2:c.216G>C	NP_001279999.1:p.Glu72Asp
NM_001293071.2:c.72G>C	NP_001280000.1:p.Glu24Asp
NM_001293072.2:c.132G>C	NP_001280001.1:p.Glu44Asp
NM_001398427.1:c.-262G>C	NP_001385356.1:n.-262G>C