Canonical Allele Identifier: CA2692848427

Gene: NSMF

Linked Data

• gnomAD v4: 9-137459083-CTGGAGGCGGCGGCGCCCATGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459085_137459105del , CM000671.2:g.137459085_137459105del	GRCh38
NC_000009.11:g.140353537_140353557del , CM000671.1:g.140353537_140353557del	GRCh37
NC_000009.10:g.139473358_139473378del	NCBI36
NG_021362.1:g.5231_5251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.-2_19del
ENST00000371475.9:c.-2_19del
ENST00000265663.11:c.-2_19del
ENST00000371472.6:c.-2_19del
ENST00000371473.7:c.-2_19del
ENST00000371474.7:c.-2_19del
ENST00000371475.7:c.-2_19del
ENST00000437259.5:c.-2_19del
NM_001130969.1:c.-2_19del
NM_001130970.1:c.-2_19del
NM_001130971.1:c.-2_19del
NM_001178064.1:c.-2_19del
NM_015537.4:c.-2_19del
XM_005266061.3:c.-2_19del
XM_005266062.3:c.-2_19del
XM_011518496.1:c.-2_19del
XM_005266061.5:c.-2_19del
XM_005266062.5:c.-2_19del
XM_011518496.3:c.-2_19del
NM_001130969.3:c.-2_19del
NM_001130970.2:c.-2_19del
NM_001130971.2:c.-2_19del
NM_001178064.2:c.-2_19del
NM_015537.5:c.-2_19del