Canonical Allele Identifier: CA1884498538

Gene: NSMF

Linked Data

• dbSNP Id: rs1831041012
• gnomAD v4: 9-137459085-GGAGGCGGCGGCGCCCATGGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459099_137459119del , CM000671.2:g.137459099_137459119del	GRCh38
NC_000009.11:g.140353551_140353571del , CM000671.1:g.140353551_140353571del	GRCh37
NC_000009.10:g.139473372_139473392del	NCBI36
NG_021362.1:g.5229_5249del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.-4_17del
ENST00000371475.9:c.-4_17del
ENST00000265663.11:c.-4_17del
ENST00000371472.6:c.-4_17del
ENST00000371473.7:c.-4_17del
ENST00000371474.7:c.-4_17del
ENST00000371475.7:c.-4_17del
ENST00000437259.5:c.-4_17del
NM_001130969.1:c.-4_17del
NM_001130970.1:c.-4_17del
NM_001130971.1:c.-4_17del
NM_001178064.1:c.-4_17del
NM_015537.4:c.-4_17del
XM_005266061.3:c.-4_17del
XM_005266062.3:c.-4_17del
XM_011518496.1:c.-4_17del
XM_005266061.5:c.-4_17del
XM_005266062.5:c.-4_17del
XM_011518496.3:c.-4_17del
NM_001130969.3:c.-4_17del
NM_001130970.2:c.-4_17del
NM_001130971.2:c.-4_17del
NM_001178064.2:c.-4_17del
NM_015537.5:c.-4_17del