Canonical Allele Identifier: CA367241741

Gene: CHN2

Linked Data

• dbSNP Id: rs1189479864
• gnomAD v2: 7-29438068-C-G
• gnomAD v4: 7-29398452-C-G
• MyVariant Identifiers: chr7:g.29438068C>G (hg19) ; chr7:g.29398452C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398452C>G , CM000669.2:g.29398452C>G	GRCh38
NC_000007.13:g.29438068C>G , CM000669.1:g.29438068C>G	GRCh37
NC_000007.12:g.29404593C>G	NCBI36
NG_029365.2:g.256906C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.295C>G	ENSP00000386968.2:p.Gln99Glu
ENST00000439384.6:n.518C>G
ENST00000446446.6:c.256C>G	ENSP00000396867.2:p.Gln86Glu
ENST00000706158.1:c.*200C>G	ENSP00000516236.1:n.*200C>G
ENST00000706159.1:c.168C>G	ENSP00000516237.1:p.Ala56=
ENST00000706160.1:c.256C>G	ENSP00000516238.1:p.Gln86Glu
ENST00000706161.1:c.334C>G	ENSP00000516239.1:p.Gln112Glu
ENST00000706162.1:c.256C>G	ENSP00000516240.1:p.Gln86Glu
ENST00000706163.1:c.50-81827C>G	ENSP00000516241.1:n.50-81827C>G
ENST00000222792.11:c.256C>G MANE Select	ENSP00000222792.7:p.Gln86Glu
ENST00000644824.1:c.481C>G	ENSP00000495614.1:p.Gln161Glu
ENST00000222792.10:c.256C>G	ENSP00000222792.6:p.Gln86Glu
ENST00000409350.5:c.295C>G	ENSP00000386968.1:p.Gln99Glu
ENST00000409922.5:n.467C>G
ENST00000409964.6:n.455C>G
ENST00000412536.5:n.276C>G
ENST00000435288.6:c.168+4750C>G	ENSP00000400282.3:n.168+4750C>G
ENST00000439384.5:c.481C>G	ENSP00000409843.1:p.Gln161Glu
ENST00000474070.5:c.356C>G
ENST00000478128.6:n.350C>G
ENST00000482820.6:n.465C>G
ENST00000491856.1:n.1805C>G
ENST00000495789.6:c.256C>G	ENSP00000438587.2:p.Gln86Glu
ENST00000539389.5:c.256C>G	ENSP00000440526.2:p.Gln86Glu
ENST00000539406.5:c.256C>G	ENSP00000444063.2:p.Gln86Glu
NM_001293069.1:c.481C>G	NP_001279998.1:p.Gln161Glu
NM_001293070.1:c.295C>G	NP_001279999.1:p.Gln99Glu
NM_001293071.1:c.151C>G	NP_001280000.1:p.Gln51Glu
NM_001293072.1:c.211C>G	NP_001280001.1:p.Gln71Glu
NM_004067.3:c.256C>G	NP_004058.1:p.Gln86Glu
XM_011515105.1:c.559C>G	XP_011513407.1:p.Gln187Glu
XM_011515106.1:c.520C>G	XP_011513408.1:p.Gln174Glu
XM_011515107.1:c.334C>G	XP_011513409.1:p.Gln112Glu
XM_011515108.1:c.256C>G	XP_011513410.1:p.Gln86Glu
XM_011515109.1:c.217C>G	XP_011513411.1:p.Gln73Glu
XM_011515110.1:c.178C>G	XP_011513412.1:p.Gln60Glu
XM_011515111.1:c.151C>G	XP_011513413.1:p.Gln51Glu
XM_011515112.1:c.559C>G	XP_011513414.1:p.Gln187Glu
XM_011515105.2:c.559C>G	XP_011513407.1:p.Gln187Glu
XM_011515106.2:c.520C>G	XP_011513408.1:p.Gln174Glu
XM_011515107.2:c.334C>G	XP_011513409.1:p.Gln112Glu
XM_017011721.1:c.577C>G	XP_016867210.1:p.Gln193Glu
XM_017011722.1:c.352C>G	XP_016867211.1:p.Gln118Glu
NM_004067.4:c.256C>G MANE Select	NP_004058.1:p.Gln86Glu
NM_001293070.2:c.295C>G	NP_001279999.1:p.Gln99Glu
NM_001293071.2:c.151C>G	NP_001280000.1:p.Gln51Glu
NM_001293072.2:c.211C>G	NP_001280001.1:p.Gln71Glu
NM_001398427.1:c.-183C>G	NP_001385356.1:n.-183C>G