Canonical Allele Identifier: CA727707407

Gene: NOS2

Linked Data

• dbSNP Id: rs1276631395
• MyVariant Identifiers: chr17:g.26096629_26096630del (hg19) ; chr17:g.27769603_27769604del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.27769604_27769605del , CM000679.2:g.27769604_27769605del	GRCh38
NC_000017.10:g.26096630_26096631del , CM000679.1:g.26096630_26096631del	GRCh37
NC_000017.9:g.23120757_23120758del	NCBI36
NG_011470.1:g.35926_35927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697337.1:c.*2546-20_*2546-19del	ENSP00000513259.1:n.*2546-20_*2546-19del
ENST00000697338.1:c.1658-20_1658-19del	ENSP00000513260.1:n.1658-20_1658-19del
ENST00000697339.1:c.844-20_844-19del	ENSP00000513261.1:n.844-20_844-19del
ENST00000697340.1:c.*527-20_*527-19del	ENSP00000513262.1:n.*527-20_*527-19del
ENST00000697341.1:n.1780-20_1780-19del
ENST00000313735.11:c.1810-20_1810-19del MANE Select	ENSP00000327251.6:n.1810-20_1810-19del
ENST00000646938.1:c.1807-20_1807-19del	ENSP00000494870.1:n.1807-20_1807-19del
ENST00000313735.10:c.1810-20_1810-19del	ENSP00000327251.6:n.1810-20_1810-19del
ENST00000621962.1:c.1693-20_1693-19del	ENSP00000482291.1:n.1693-20_1693-19del
NM_000625.4:c.1810-20_1810-19del MANE Select	NP_000616.3:n.1810-20_1810-19del
XM_011524859.1:c.1810-20_1810-19del	XP_011523161.1:n.1810-20_1810-19del
XM_011524860.1:c.1807-20_1807-19del	XP_011523162.1:n.1807-20_1807-19del
XM_011524861.1:c.1810-20_1810-19del	XP_011523163.1:n.1810-20_1810-19del
XM_011524862.1:c.1144-20_1144-19del	XP_011523164.1:n.1144-20_1144-19del