Canonical Allele Identifier: CA375754217

Gene: NSMF

Linked Data

• MyVariant Identifiers: chr9:g.140344115G>C (hg19) ; chr9:g.137449663G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137449663G>C , CM000671.2:g.137449663G>C	GRCh38
NC_000009.11:g.140344115G>C , CM000671.1:g.140344115G>C	GRCh37
NC_000009.10:g.139463936G>C	NCBI36
NG_021362.1:g.14672C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265663.12:c.1425C>G	ENSP00000265663.7:p.Asn475Lys
ENST00000371475.9:c.1431C>G MANE Select	ENSP00000360530.3:p.Asn477Lys
ENST00000265663.11:c.1425C>G	ENSP00000265663.7:p.Asn475Lys
ENST00000339554.7:c.822C>G	ENSP00000342966.3:p.Asn274Lys
ENST00000371472.6:c.1425C>G	ENSP00000360527.1:p.Asn475Lys
ENST00000371473.7:c.1341C>G	ENSP00000360528.3:p.Asn447Lys
ENST00000371474.7:c.1356C>G	ENSP00000360529.3:p.Asn452Lys
ENST00000371475.7:c.1431C>G	ENSP00000360530.3:p.Asn477Lys
ENST00000371482.5:c.423C>G	ENSP00000360537.1:p.Asn141Lys
ENST00000437259.5:c.1362C>G	ENSP00000412007.1:p.Asn454Lys
ENST00000484316.5:n.877C>G
NM_001130969.1:c.1431C>G	NP_001124441.1:p.Asn477Lys
NM_001130970.1:c.1362C>G	NP_001124442.1:p.Asn454Lys
NM_001130971.1:c.1356C>G	NP_001124443.1:p.Asn452Lys
NM_001178064.1:c.1341C>G	NP_001171535.1:p.Asn447Lys
NM_015537.4:c.1425C>G	NP_056352.3:p.Asn475Lys
XM_005266061.3:c.1335C>G	XP_005266118.1:p.Asn445Lys
XM_005266062.3:c.1266C>G	XP_005266119.1:p.Asn422Lys
XM_011518496.1:c.1272C>G	XP_011516798.1:p.Asn424Lys
XM_011518497.1:c.630C>G	XP_011516799.1:p.Asn210Lys
XM_005266061.5:c.1335C>G	XP_005266118.1:p.Asn445Lys
XM_005266062.5:c.1266C>G	XP_005266119.1:p.Asn422Lys
XM_011518496.3:c.1272C>G	XP_011516798.1:p.Asn424Lys
XM_011518497.2:c.630C>G	XP_011516799.1:p.Asn210Lys
XM_017014597.2:c.903C>G	XP_016870086.1:p.Asn301Lys
NM_001130969.3:c.1431C>G MANE Select	NP_001124441.1:p.Asn477Lys
NM_001130970.2:c.1362C>G	NP_001124442.1:p.Asn454Lys
NM_001130971.2:c.1356C>G	NP_001124443.1:p.Asn452Lys
NM_001178064.2:c.1341C>G	NP_001171535.1:p.Asn447Lys
NM_015537.5:c.1425C>G	NP_056352.3:p.Asn475Lys