Canonical Allele Identifier: CA2692848439

Gene: NSMF

Linked Data

• gnomAD v4: 9-137459099-CCATGGTCGAGGCGGCGGCGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459100_137459120del , CM000671.2:g.137459100_137459120del	GRCh38
NC_000009.11:g.140353552_140353572del , CM000671.1:g.140353552_140353572del	GRCh37
NC_000009.10:g.139473373_139473393del	NCBI36
NG_021362.1:g.5215_5235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.-18_3del
ENST00000371475.9:c.-18_3del
ENST00000265663.11:c.-18_3del
ENST00000371472.6:c.-18_3del
ENST00000371473.7:c.-18_3del
ENST00000371474.7:c.-18_3del
ENST00000371475.7:c.-18_3del
ENST00000437259.5:c.-18_3del
NM_001130969.1:c.-18_3del
NM_001130970.1:c.-18_3del
NM_001130971.1:c.-18_3del
NM_001178064.1:c.-18_3del
NM_015537.4:c.-18_3del
XM_005266061.3:c.-18_3del
XM_005266062.3:c.-18_3del
XM_011518496.1:c.-18_3del
XM_005266061.5:c.-18_3del
XM_005266062.5:c.-18_3del
XM_011518496.3:c.-18_3del
NM_001130969.3:c.-18_3del
NM_001130970.2:c.-18_3del
NM_001130971.2:c.-18_3del
NM_001178064.2:c.-18_3del
NM_015537.5:c.-18_3del