Canonical Allele Identifier: CA375772605
Gene: NSMF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137459075C>T , CM000671.2:g.137459075C>T GRCh38
NC_000009.11:g.140353527C>T , CM000671.1:g.140353527C>T GRCh37
NC_000009.10:g.139473348C>T NCBI36
NG_021362.1:g.5260G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265663.12:c.28G>A ENSP00000265663.7:p.Ala10Thr
ENST00000371475.9:c.28G>A MANE Select ENSP00000360530.3:p.Ala10Thr
ENST00000265663.11:c.28G>A ENSP00000265663.7:p.Ala10Thr
ENST00000371472.6:c.28G>A ENSP00000360527.1:p.Ala10Thr
ENST00000371473.7:c.28G>A ENSP00000360528.3:p.Ala10Thr
ENST00000371474.7:c.28G>A ENSP00000360529.3:p.Ala10Thr
ENST00000371475.7:c.28G>A ENSP00000360530.3:p.Ala10Thr
ENST00000437259.5:c.28G>A ENSP00000412007.1:p.Ala10Thr
NM_001130969.1:c.28G>A NP_001124441.1:p.Ala10Thr
NM_001130970.1:c.28G>A NP_001124442.1:p.Ala10Thr
NM_001130971.1:c.28G>A NP_001124443.1:p.Ala10Thr
NM_001178064.1:c.28G>A NP_001171535.1:p.Ala10Thr
NM_015537.4:c.28G>A NP_056352.3:p.Ala10Thr
XM_005266061.3:c.28G>A XP_005266118.1:p.Ala10Thr
XM_005266062.3:c.28G>A XP_005266119.1:p.Ala10Thr
XM_011518496.1:c.28G>A XP_011516798.1:p.Ala10Thr
XM_005266061.5:c.28G>A XP_005266118.1:p.Ala10Thr
XM_005266062.5:c.28G>A XP_005266119.1:p.Ala10Thr
XM_011518496.3:c.28G>A XP_011516798.1:p.Ala10Thr
NM_001130969.3:c.28G>A MANE Select NP_001124441.1:p.Ala10Thr
NM_001130970.2:c.28G>A NP_001124442.1:p.Ala10Thr
NM_001130971.2:c.28G>A NP_001124443.1:p.Ala10Thr
NM_001178064.2:c.28G>A NP_001171535.1:p.Ala10Thr
NM_015537.5:c.28G>A NP_056352.3:p.Ala10Thr