Canonical Allele Identifier: CA2254008441

Gene: NOS2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769586_27769590delinsTAGAA , CM000679.2:g.27769586_27769590delinsTAGAA	GRCh38
NC_000017.10:g.26096612_26096616delinsTAGAA , CM000679.1:g.26096612_26096616delinsTAGAA	GRCh37
NC_000017.9:g.23120739_23120743delinsTAGAA	NCBI36
NG_011470.1:g.35940_35944delinsTTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2546-6_*2546-2delinsTTCTA	ENSP00000513259.1:n.*2546-6_*2546-2delinsTTCTA
ENST00000697338.1:c.1658-6_1658-2delinsTTCTA	ENSP00000513260.1:n.1658-6_1658-2delinsTTCTA
ENST00000697339.1:c.844-6_844-2delinsTTCTA	ENSP00000513261.1:n.844-6_844-2delinsTTCTA
ENST00000697340.1:c.*527-6_*527-2delinsTTCTA	ENSP00000513262.1:n.*527-6_*527-2delinsTTCTA
ENST00000697341.1:n.1780-6_1780-2delinsTTCTA
ENST00000313735.11:c.1810-6_1810-2delinsTTCTA MANE Select	ENSP00000327251.6:n.1810-6_1810-2delinsTTCTA
ENST00000646938.1:c.1807-6_1807-2delinsTTCTA	ENSP00000494870.1:n.1807-6_1807-2delinsTTCTA
ENST00000313735.10:c.1810-6_1810-2delinsTTCTA	ENSP00000327251.6:n.1810-6_1810-2delinsTTCTA
ENST00000621962.1:c.1693-6_1693-2delinsTTCTA	ENSP00000482291.1:n.1693-6_1693-2delinsTTCTA
NM_000625.4:c.1810-6_1810-2delinsTTCTA MANE Select	NP_000616.3:n.1810-6_1810-2delinsTTCTA
XM_011524859.1:c.1810-6_1810-2delinsTTCTA	XP_011523161.1:n.1810-6_1810-2delinsTTCTA
XM_011524860.1:c.1807-6_1807-2delinsTTCTA	XP_011523162.1:n.1807-6_1807-2delinsTTCTA
XM_011524861.1:c.1810-6_1810-2delinsTTCTA	XP_011523163.1:n.1810-6_1810-2delinsTTCTA
XM_011524862.1:c.1144-6_1144-2delinsTTCTA	XP_011523164.1:n.1144-6_1144-2delinsTTCTA