Canonical Allele Identifier: CA2254005145
Gene: NOS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27761762_27761770delinsCCTGGGCTT , CM000679.2:g.27761762_27761770delinsCCTGGGCTT GRCh38
NC_000017.10:g.26088788_26088796delinsCCTGGGCTT , CM000679.1:g.26088788_26088796delinsCCTGGGCTT GRCh37
NC_000017.9:g.23112915_23112923delinsCCTGGGCTT NCBI36
NG_011470.1:g.43760_43768delinsAAGCCCAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000697337.1:c.*3465-539_*3465-531delinsAAGCCCAGG ENSP00000513259.1:n.*3465-539_*3465-531de...
ENST00000697338.1:c.2649-539_2649-531delinsAAGCCCAGG ENSP00000513260.1:n.2649-539_2649-531deli...
ENST00000697339.1:c.1763-539_1763-531delinsAAGCCCAGG ENSP00000513261.1:n.1763-539_1763-531deli...
ENST00000697340.1:c.*1514-539_*1514-531delinsAAGCCCAGG ENSP00000513262.1:n.*1514-539_*1514-531de...
ENST00000313735.11:c.2801-539_2801-531delinsAAGCCCAGG MANE Select ENSP00000327251.6:n.2801-539_2801-531deli...
ENST00000646938.1:c.2798-539_2798-531delinsAAGCCCAGG ENSP00000494870.1:n.2798-539_2798-531deli...
ENST00000313735.10:c.2801-539_2801-531delinsAAGCCCAGG ENSP00000327251.6:n.2801-539_2801-531deli...
ENST00000621962.1:c.2684-539_2684-531delinsAAGCCCAGG ENSP00000482291.1:n.2684-539_2684-531deli...
NM_000625.4:c.2801-539_2801-531delinsAAGCCCAGG MANE Select NP_000616.3:n.2801-539_2801-531delinsAAGC...
XM_011524859.1:c.2801-539_2801-531delinsAAGCCCAGG XP_011523161.1:n.2801-539_2801-531delinsA...
XM_011524860.1:c.2798-539_2798-531delinsAAGCCCAGG XP_011523162.1:n.2798-539_2798-531delinsA...
XM_011524861.1:c.2729-539_2729-531delinsAAGCCCAGG XP_011523163.1:n.2729-539_2729-531delinsA...
XM_011524862.1:c.2135-539_2135-531delinsAAGCCCAGG XP_011523164.1:n.2135-539_2135-531delinsA...