Canonical Allele Identifier: CA1884498526

Gene: NSMF

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459064G= , CM000671.2:g.137459064G=	GRCh38
NC_000009.11:g.140353516G= , CM000671.1:g.140353516G=	GRCh37
NC_000009.10:g.139473337G=	NCBI36
NG_021362.1:g.5271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.39C=	ENSP00000265663.7:p.Ser13=
ENST00000371475.9:c.39C= MANE Select	ENSP00000360530.3:p.Ser13=
ENST00000265663.11:c.39C=	ENSP00000265663.7:p.Ser13=
ENST00000371472.6:c.39C=	ENSP00000360527.1:p.Ser13=
ENST00000371473.7:c.39C=	ENSP00000360528.3:p.Ser13=
ENST00000371474.7:c.39C=	ENSP00000360529.3:p.Ser13=
ENST00000371475.7:c.39C=	ENSP00000360530.3:p.Ser13=
ENST00000437259.5:c.39C=	ENSP00000412007.1:p.Ser13=
NM_001130969.1:c.39C=	NP_001124441.1:p.Ser13=
NM_001130970.1:c.39C=	NP_001124442.1:p.Ser13=
NM_001130971.1:c.39C=	NP_001124443.1:p.Ser13=
NM_001178064.1:c.39C=	NP_001171535.1:p.Ser13=
NM_015537.4:c.39C=	NP_056352.3:p.Ser13=
XM_005266061.3:c.39C=	XP_005266118.1:p.Ser13=
XM_005266062.3:c.39C=	XP_005266119.1:p.Ser13=
XM_011518496.1:c.39C=	XP_011516798.1:p.Ser13=
XM_005266061.5:c.39C=	XP_005266118.1:p.Ser13=
XM_005266062.5:c.39C=	XP_005266119.1:p.Ser13=
XM_011518496.3:c.39C=	XP_011516798.1:p.Ser13=
NM_001130969.3:c.39C= MANE Select	NP_001124441.1:p.Ser13=
NM_001130970.2:c.39C=	NP_001124442.1:p.Ser13=
NM_001130971.2:c.39C=	NP_001124443.1:p.Ser13=
NM_001178064.2:c.39C=	NP_001171535.1:p.Ser13=
NM_015537.5:c.39C=	NP_056352.3:p.Ser13=