Canonical Allele Identifier: CA14474155
Gene: FLOT2 HGNC NCBI

Linked Data

dbSNP Id: rs10205

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.28880102G>A , CM000679.2:g.28880102G>A GRCh38
NC_000017.10:g.27207120G>A , CM000679.1:g.27207120G>A GRCh37
NC_000017.9:g.24231246G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000585169.6:c.*459C>T ENSP00000463503.1:n.*459C>T
ENST00000394908.9:c.*459C>T MANE Select ENSP00000378368.3:n.*459C>T
ENST00000394906.6:c.*459C>T ENSP00000378366.2:n.*459C>T
ENST00000394908.8:c.*459C>T ENSP00000378368.3:n.*459C>T
ENST00000577789.5:n.1742C>T
ENST00000580805.5:c.*1480C>T ENSP00000463304.1:n.*1480C>T
ENST00000584569.1:n.88-583C>T
ENST00000585169.5:c.*459C>T ENSP00000463503.1:n.*459C>T
NM_004475.2:c.*459C>T NP_004466.2:n.*459C>T
XM_005257950.2:c.*459C>T XP_005258007.1:n.*459C>T
XM_005257952.1:c.*459C>T XP_005258009.1:n.*459C>T
XM_005257953.1:c.*459C>T XP_005258010.1:n.*459C>T
NM_001330170.1:c.*459C>T NP_001317099.1:n.*459C>T
XM_005257953.2:c.*459C>T XP_005258010.1:n.*459C>T
XM_017024394.1:c.*459C>T XP_016879883.1:n.*459C>T
XM_017024395.1:c.*459C>T XP_016879884.1:n.*459C>T
XM_017024396.1:c.*459C>T XP_016879885.1:n.*459C>T
XM_024450666.1:c.*459C>T XP_024306434.1:n.*459C>T
XM_024450667.1:c.*459C>T XP_024306435.1:n.*459C>T
NM_004475.3:c.*459C>T MANE Select NP_004466.2:n.*459C>T
NM_001330170.2:c.*459C>T NP_001317099.1:n.*459C>T