Canonical Allele Identifier: CA2692848465

Gene: NSMF

Linked Data

• gnomAD v4: 9-137459113-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459113G>A , CM000671.2:g.137459113G>A	GRCh38
NC_000009.11:g.140353565G>A , CM000671.1:g.140353565G>A	GRCh37
NC_000009.10:g.139473386G>A	NCBI36
NG_021362.1:g.5222C>T

Transcript Alleles

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