Canonical Allele Identifier: CA467869716

Gene: NSMF

Linked Data

• MyVariant Identifiers: chr9:g.140353486C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459034C>G , CM000671.2:g.137459034C>G	GRCh38
NC_000009.11:g.140353486C>G , CM000671.1:g.140353486C>G	GRCh37
NC_000009.10:g.139473307C>G	NCBI36
NG_021362.1:g.5301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.69G>C	ENSP00000265663.7:p.Val23=
ENST00000371475.9:c.69G>C MANE Select	ENSP00000360530.3:p.Val23=
ENST00000265663.11:c.69G>C	ENSP00000265663.7:p.Val23=
ENST00000371472.6:c.69G>C	ENSP00000360527.1:p.Val23=
ENST00000371473.7:c.69G>C	ENSP00000360528.3:p.Val23=
ENST00000371474.7:c.69G>C	ENSP00000360529.3:p.Val23=
ENST00000371475.7:c.69G>C	ENSP00000360530.3:p.Val23=
ENST00000437259.5:c.69G>C	ENSP00000412007.1:p.Val23=
NM_001130969.1:c.69G>C	NP_001124441.1:p.Val23=
NM_001130970.1:c.69G>C	NP_001124442.1:p.Val23=
NM_001130971.1:c.69G>C	NP_001124443.1:p.Val23=
NM_001178064.1:c.69G>C	NP_001171535.1:p.Val23=
NM_015537.4:c.69G>C	NP_056352.3:p.Val23=
XM_005266061.3:c.69G>C	XP_005266118.1:p.Val23=
XM_005266062.3:c.69G>C	XP_005266119.1:p.Val23=
XM_011518496.1:c.69G>C	XP_011516798.1:p.Val23=
XM_005266061.5:c.69G>C	XP_005266118.1:p.Val23=
XM_005266062.5:c.69G>C	XP_005266119.1:p.Val23=
XM_011518496.3:c.69G>C	XP_011516798.1:p.Val23=
NM_001130969.3:c.69G>C MANE Select	NP_001124441.1:p.Val23=
NM_001130970.2:c.69G>C	NP_001124442.1:p.Val23=
NM_001130971.2:c.69G>C	NP_001124443.1:p.Val23=
NM_001178064.2:c.69G>C	NP_001171535.1:p.Val23=
NM_015537.5:c.69G>C	NP_056352.3:p.Val23=