Canonical Allele Identifier: CA454421620

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438079A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398463A>G , CM000669.2:g.29398463A>G	GRCh38
NC_000007.13:g.29438079A>G , CM000669.1:g.29438079A>G	GRCh37
NC_000007.12:g.29404604A>G	NCBI36
NG_029365.2:g.256917A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.306A>G	ENSP00000386968.2:p.Pro102=
ENST00000439384.6:n.529A>G
ENST00000446446.6:c.267A>G	ENSP00000396867.2:p.Pro89=
ENST00000706158.1:c.*211A>G	ENSP00000516236.1:n.*211A>G
ENST00000706159.1:c.179A>G	ENSP00000516237.1:p.Gln60Arg
ENST00000706160.1:c.267A>G	ENSP00000516238.1:p.Pro89=
ENST00000706161.1:c.345A>G	ENSP00000516239.1:p.Pro115=
ENST00000706162.1:c.267A>G	ENSP00000516240.1:p.Pro89=
ENST00000706163.1:c.50-81816A>G	ENSP00000516241.1:n.50-81816A>G
ENST00000222792.11:c.267A>G MANE Select	ENSP00000222792.7:p.Pro89=
ENST00000644824.1:c.492A>G	ENSP00000495614.1:p.Pro164=
ENST00000222792.10:c.267A>G	ENSP00000222792.6:p.Pro89=
ENST00000409350.5:c.306A>G	ENSP00000386968.1:p.Pro102=
ENST00000409922.5:n.478A>G
ENST00000409964.6:n.466A>G
ENST00000412536.5:n.287A>G
ENST00000435288.6:c.168+4761A>G	ENSP00000400282.3:n.168+4761A>G
ENST00000439384.5:c.492A>G	ENSP00000409843.1:p.Pro164=
ENST00000474070.5:c.367A>G
ENST00000478128.6:n.361A>G
ENST00000482820.6:n.476A>G
ENST00000491856.1:n.1816A>G
ENST00000495789.6:c.267A>G	ENSP00000438587.2:p.Pro89=
ENST00000539389.5:c.267A>G	ENSP00000440526.2:p.Pro89=
ENST00000539406.5:c.267A>G	ENSP00000444063.2:p.Pro89=
NM_001293069.1:c.492A>G	NP_001279998.1:p.Pro164=
NM_001293070.1:c.306A>G	NP_001279999.1:p.Pro102=
NM_001293071.1:c.162A>G	NP_001280000.1:p.Pro54=
NM_001293072.1:c.222A>G	NP_001280001.1:p.Pro74=
NM_004067.3:c.267A>G	NP_004058.1:p.Pro89=
XM_011515105.1:c.570A>G	XP_011513407.1:p.Pro190=
XM_011515106.1:c.531A>G	XP_011513408.1:p.Pro177=
XM_011515107.1:c.345A>G	XP_011513409.1:p.Pro115=
XM_011515108.1:c.267A>G	XP_011513410.1:p.Pro89=
XM_011515109.1:c.228A>G	XP_011513411.1:p.Pro76=
XM_011515110.1:c.189A>G	XP_011513412.1:p.Pro63=
XM_011515111.1:c.162A>G	XP_011513413.1:p.Pro54=
XM_011515112.1:c.570A>G	XP_011513414.1:p.Pro190=
XM_011515105.2:c.570A>G	XP_011513407.1:p.Pro190=
XM_011515106.2:c.531A>G	XP_011513408.1:p.Pro177=
XM_011515107.2:c.345A>G	XP_011513409.1:p.Pro115=
XM_017011721.1:c.588A>G	XP_016867210.1:p.Pro196=
XM_017011722.1:c.363A>G	XP_016867211.1:p.Pro121=
NM_004067.4:c.267A>G MANE Select	NP_004058.1:p.Pro89=
NM_001293070.2:c.306A>G	NP_001279999.1:p.Pro102=
NM_001293071.2:c.162A>G	NP_001280000.1:p.Pro54=
NM_001293072.2:c.222A>G	NP_001280001.1:p.Pro74=
NM_001398427.1:c.-172A>G	NP_001385356.1:n.-172A>G