Canonical Allele Identifier: CA467868369

Gene: NSMF

Linked Data

• MyVariant Identifiers: chr9:g.140344111T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137449659T>G , CM000671.2:g.137449659T>G	GRCh38
NC_000009.11:g.140344111T>G , CM000671.1:g.140344111T>G	GRCh37
NC_000009.10:g.139463932T>G	NCBI36
NG_021362.1:g.14676A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265663.12:c.1429A>C	ENSP00000265663.7:p.Arg477=
ENST00000371475.9:c.1435A>C MANE Select	ENSP00000360530.3:p.Arg479=
ENST00000265663.11:c.1429A>C	ENSP00000265663.7:p.Arg477=
ENST00000339554.7:c.826A>C	ENSP00000342966.3:p.Arg276=
ENST00000371472.6:c.1429A>C	ENSP00000360527.1:p.Arg477=
ENST00000371473.7:c.1345A>C	ENSP00000360528.3:p.Arg449=
ENST00000371474.7:c.1360A>C	ENSP00000360529.3:p.Arg454=
ENST00000371475.7:c.1435A>C	ENSP00000360530.3:p.Arg479=
ENST00000371482.5:c.427A>C	ENSP00000360537.1:p.Arg143=
ENST00000437259.5:c.1366A>C	ENSP00000412007.1:p.Arg456=
ENST00000484316.5:n.881A>C
NM_001130969.1:c.1435A>C	NP_001124441.1:p.Arg479=
NM_001130970.1:c.1366A>C	NP_001124442.1:p.Arg456=
NM_001130971.1:c.1360A>C	NP_001124443.1:p.Arg454=
NM_001178064.1:c.1345A>C	NP_001171535.1:p.Arg449=
NM_015537.4:c.1429A>C	NP_056352.3:p.Arg477=
XM_005266061.3:c.1339A>C	XP_005266118.1:p.Arg447=
XM_005266062.3:c.1270A>C	XP_005266119.1:p.Arg424=
XM_011518496.1:c.1276A>C	XP_011516798.1:p.Arg426=
XM_011518497.1:c.634A>C	XP_011516799.1:p.Arg212=
XM_005266061.5:c.1339A>C	XP_005266118.1:p.Arg447=
XM_005266062.5:c.1270A>C	XP_005266119.1:p.Arg424=
XM_011518496.3:c.1276A>C	XP_011516798.1:p.Arg426=
XM_011518497.2:c.634A>C	XP_011516799.1:p.Arg212=
XM_017014597.2:c.907A>C	XP_016870086.1:p.Arg303=
NM_001130969.3:c.1435A>C MANE Select	NP_001124441.1:p.Arg479=
NM_001130970.2:c.1366A>C	NP_001124442.1:p.Arg456=
NM_001130971.2:c.1360A>C	NP_001124443.1:p.Arg454=
NM_001178064.2:c.1345A>C	NP_001171535.1:p.Arg449=
NM_015537.5:c.1429A>C	NP_056352.3:p.Arg477=