Canonical Allele Identifier: CA246010

Gene: FSCN2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81537084C>T , CM000679.2:g.81537084C>T	GRCh38
NC_000017.10:g.79504110C>T , CM000679.1:g.79504110C>T	GRCh37
NC_000017.9:g.77114586C>T	NCBI36
NG_015964.1:g.13694C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012418.4:c.*4C>T MANE Select	NP_036550.1:n.*4C>T
ENST00000417245.7:c.*4C>T MANE Select	ENSP00000388716.2:n.*4C>T
NM_001077182.2:c.*4C>T	NP_001070650.1:n.*4C>T
NM_001077182.3:c.*4C>T	NP_001070650.1:n.*4C>T
NM_012418.3:c.*4C>T	NP_036550.1:n.*4C>T
ENST00000417245.6:c.*4C>T	ENSP00000388716.2:n.*4C>T
XM_005257195.3:c.*4C>T	XP_005257252.1:n.*4C>T
XM_011524587.1:c.*4C>T	XP_011522889.1:n.*4C>T
XM_011524587.2:c.*4C>T	XP_011522889.1:n.*4C>T
XM_011524588.1:c.*4C>T	XP_011522890.1:n.*4C>T
XM_011524589.1:c.*4C>T	XP_011522891.1:n.*4C>T
XM_011524590.1:c.*4C>T	XP_011522892.1:n.*4C>T
XM_011524590.2:c.*4C>T	XP_011522892.1:n.*4C>T
XM_011524591.1:c.*4C>T	XP_011522893.1:n.*4C>T
XM_011524592.1:c.*4C>T	XP_011522894.1:n.*4C>T
XM_011524593.1:c.*4C>T	XP_011522895.1:n.*4C>T
XM_011524594.1:c.*4C>T	XP_011522896.1:n.*4C>T