Canonical Allele Identifier: CA1884492714

Gene: NSMF

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137449656T= , CM000671.2:g.137449656T=	GRCh38
NC_000009.11:g.140344108T= , CM000671.1:g.140344108T=	GRCh37
NC_000009.10:g.139463929T=	NCBI36
NG_021362.1:g.14679A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265663.12:c.1432A=	ENSP00000265663.7:p.Thr478=
ENST00000371475.9:c.1438A= MANE Select	ENSP00000360530.3:p.Thr480=
ENST00000265663.11:c.1432A=	ENSP00000265663.7:p.Thr478=
ENST00000339554.7:c.829A=	ENSP00000342966.3:p.Thr277=
ENST00000371472.6:c.1432A=	ENSP00000360527.1:p.Thr478=
ENST00000371473.7:c.1348A=	ENSP00000360528.3:p.Thr450=
ENST00000371474.7:c.1363A=	ENSP00000360529.3:p.Thr455=
ENST00000371475.7:c.1438A=	ENSP00000360530.3:p.Thr480=
ENST00000371482.5:c.430A=	ENSP00000360537.1:p.Thr144=
ENST00000437259.5:c.1369A=	ENSP00000412007.1:p.Thr457=
ENST00000484316.5:n.884A=
NM_001130969.1:c.1438A=	NP_001124441.1:p.Thr480=
NM_001130970.1:c.1369A=	NP_001124442.1:p.Thr457=
NM_001130971.1:c.1363A=	NP_001124443.1:p.Thr455=
NM_001178064.1:c.1348A=	NP_001171535.1:p.Thr450=
NM_015537.4:c.1432A=	NP_056352.3:p.Thr478=
XM_005266061.3:c.1342A=	XP_005266118.1:p.Thr448=
XM_005266062.3:c.1273A=	XP_005266119.1:p.Thr425=
XM_011518496.1:c.1279A=	XP_011516798.1:p.Thr427=
XM_011518497.1:c.637A=	XP_011516799.1:p.Thr213=
XM_005266061.5:c.1342A=	XP_005266118.1:p.Thr448=
XM_005266062.5:c.1273A=	XP_005266119.1:p.Thr425=
XM_011518496.3:c.1279A=	XP_011516798.1:p.Thr427=
XM_011518497.2:c.637A=	XP_011516799.1:p.Thr213=
XM_017014597.2:c.910A=	XP_016870086.1:p.Thr304=
NM_001130969.3:c.1438A= MANE Select	NP_001124441.1:p.Thr480=
NM_001130970.2:c.1369A=	NP_001124442.1:p.Thr457=
NM_001130971.2:c.1363A=	NP_001124443.1:p.Thr455=
NM_001178064.2:c.1348A=	NP_001171535.1:p.Thr450=
NM_015537.5:c.1432A=	NP_056352.3:p.Thr478=