Canonical Allele Identifier: CA2254013134

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27779586G= , CM000679.2:g.27779586G=	GRCh38
NC_000017.10:g.26106612G= , CM000679.1:g.26106612G=	GRCh37
NC_000017.9:g.23130739G=	NCBI36
NG_011470.1:g.25944C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697337.1:c.*451-530C=	ENSP00000513259.1:n.*451-530C=
ENST00000697338.1:c.853-530C=	ENSP00000513260.1:n.853-530C=
ENST00000697339.1:c.316-5135C=	ENSP00000513261.1:n.316-5135C=
ENST00000697340.1:c.1002-530C=	ENSP00000513262.1:n.1002-530C=
ENST00000697341.1:n.975-530C=
ENST00000313735.11:c.1005-530C= MANE Select	ENSP00000327251.6:n.1005-530C=
ENST00000646938.1:c.1002-530C=	ENSP00000494870.1:n.1002-530C=
ENST00000313735.10:c.1005-530C=	ENSP00000327251.6:n.1005-530C=
ENST00000621962.1:c.888-530C=	ENSP00000482291.1:n.888-530C=
NM_000625.4:c.1005-530C= MANE Select	NP_000616.3:n.1005-530C=
XM_011524859.1:c.1005-530C=	XP_011523161.1:n.1005-530C=
XM_011524860.1:c.1002-530C=	XP_011523162.1:n.1002-530C=
XM_011524861.1:c.1005-530C=	XP_011523163.1:n.1005-530C=
XM_011524862.1:c.339-530C=	XP_011523164.1:n.339-530C=