Canonical Allele Identifier: CA201765167

Gene: NSMF

Linked Data

• dbSNP Id: rs1016789434
• gnomAD v3: 9-137459028-T-G
• gnomAD v4: 9-137459028-T-G
• MyVariant Identifiers: chr9:g.140353480T>G (hg19) ; chr9:g.137459028T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137459028T>G , CM000671.2:g.137459028T>G	GRCh38
NC_000009.11:g.140353480T>G , CM000671.1:g.140353480T>G	GRCh37
NC_000009.10:g.139473301T>G	NCBI36
NG_021362.1:g.5307A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265663.12:c.71+4A>C	ENSP00000265663.7:n.71+4A>C
ENST00000371475.9:c.71+4A>C MANE Select	ENSP00000360530.3:n.71+4A>C
ENST00000265663.11:c.71+4A>C	ENSP00000265663.7:n.71+4A>C
ENST00000371472.6:c.71+4A>C	ENSP00000360527.1:n.71+4A>C
ENST00000371473.7:c.71+4A>C	ENSP00000360528.3:n.71+4A>C
ENST00000371474.7:c.71+4A>C	ENSP00000360529.3:n.71+4A>C
ENST00000371475.7:c.71+4A>C	ENSP00000360530.3:n.71+4A>C
ENST00000437259.5:c.71+4A>C	ENSP00000412007.1:n.71+4A>C
NM_001130969.1:c.71+4A>C	NP_001124441.1:n.71+4A>C
NM_001130970.1:c.71+4A>C	NP_001124442.1:n.71+4A>C
NM_001130971.1:c.71+4A>C	NP_001124443.1:n.71+4A>C
NM_001178064.1:c.71+4A>C	NP_001171535.1:n.71+4A>C
NM_015537.4:c.71+4A>C	NP_056352.3:n.71+4A>C
XM_005266061.3:c.71+4A>C	XP_005266118.1:n.71+4A>C
XM_005266062.3:c.71+4A>C	XP_005266119.1:n.71+4A>C
XM_011518496.1:c.71+4A>C	XP_011516798.1:n.71+4A>C
XM_005266061.5:c.71+4A>C	XP_005266118.1:n.71+4A>C
XM_005266062.5:c.71+4A>C	XP_005266119.1:n.71+4A>C
XM_011518496.3:c.71+4A>C	XP_011516798.1:n.71+4A>C
NM_001130969.3:c.71+4A>C MANE Select	NP_001124441.1:n.71+4A>C
NM_001130970.2:c.71+4A>C	NP_001124442.1:n.71+4A>C
NM_001130971.2:c.71+4A>C	NP_001124443.1:n.71+4A>C
NM_001178064.2:c.71+4A>C	NP_001171535.1:n.71+4A>C
NM_015537.5:c.71+4A>C	NP_056352.3:n.71+4A>C