Canonical Allele Identifier: CA32532236
Gene: FMO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171199445_171199446delinsTG , CM000663.2:g.171199445_171199446delinsTG GRCh38
NC_000001.10:g.171168584_171168585delinsTG , CM000663.1:g.171168584_171168585delinsTG GRCh37
NC_000001.9:g.169435208_169435209delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000209929.10:c.584_585delinsTG MANE Select ENSP00000209929.8:p.Ser195Leu
ENST00000209929.9:c.584_585delinsTG ENSP00000209929.8:p.Ser195Leu
ENST00000489354.3:n.349_350delinsTG
ENST00000529935.5:c.412+2634_412+2635delinsTG ENSP00000487002.1:n.412+2634_412+2635delinsTG
NM_001301347.1:c.-34+2634_-34+2635delinsTG NP_001288276.1:n.-34+2634_-34+2635delinsTG
NM_001460.4:c.584_585delinsTG NP_001451.2:p.Ser195Leu
XR_426768.2:n.701_702delinsTG
XR_921761.1:n.701_702delinsTG
XR_922278.1:n.508-31258_508-31257delinsCA
NM_001365900.1:c.389_390delinsTG NP_001352829.1:p.Ser130Leu
NR_158622.1:n.604_605delinsTG
XR_001737072.2:n.651_652delinsTG
XR_001738291.2:n.1307-31258_1307-31257delinsCA
XR_921761.3:n.651_652delinsTG
XR_922278.3:n.1307-31258_1307-31257delinsCA
NM_001460.5:c.584_585delinsTG MANE Select NP_001451.2:p.Ser195Leu
NR_160266.1:n.512_513delinsTG
NM_001301347.2:c.-34+2634_-34+2635delinsTG NP_001288276.1:n.-34+2634_-34+2635delinsTG