Canonical Allele Identifier: CA398378799

Gene: ZSWIM7

Linked Data

• MyVariant Identifiers: chr17:g.15897092A>C (hg19) ; chr17:g.15993778A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15993778A>C , CM000679.2:g.15993778A>C	GRCh38
NC_000017.10:g.15897092A>C , CM000679.1:g.15897092A>C	GRCh37
NC_000017.9:g.15837817A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399277.6:c.77T>G MANE Select	ENSP00000382218.1:p.Ile26Ser
ENST00000399277.5:c.77T>G	ENSP00000382218.1:p.Ile26Ser
ENST00000399280.6:n.36T>G
ENST00000460252.5:c.93T>G	ENSP00000464463.1:p.Ser31=
ENST00000460315.5:c.93T>G	ENSP00000462590.1:p.Ser31=
ENST00000472495.5:c.77T>G	ENSP00000419138.1:p.Ile26Ser
ENST00000474716.5:c.90T>G	ENSP00000464500.1:p.Ser30Arg
ENST00000475498.5:n.53T>G
ENST00000476496.5:c.87T>G	ENSP00000462208.1:p.Ser29=
ENST00000486655.5:c.32T>G	ENSP00000464371.1:p.Ile11Ser
ENST00000486706.6:c.90T>G	ENSP00000463327.1:p.Ser30Arg
ENST00000490395.5:c.90T>G	ENSP00000464605.1:p.Ser30Arg
ENST00000491631.5:c.90T>G	ENSP00000462598.1:p.Ser30Arg
ENST00000495825.6:n.25T>G
ENST00000497719.5:n.55T>G
ENST00000579955.1:c.89+5728T>G	ENSP00000463444.1:n.89+5728T>G
ENST00000584519.5:c.76+5741T>G	ENSP00000463592.1:n.76+5741T>G
ENST00000585208.5:c.90T>G	ENSP00000464227.1:p.Ser30Arg
NM_001042697.1:c.77T>G	NP_001036162.1:p.Ile26Ser
NM_001042698.1:c.77T>G	NP_001036163.1:p.Ile26Ser
NM_001042697.2:c.77T>G MANE Select	NP_001036162.1:p.Ile26Ser
NM_001042698.2:c.77T>G	NP_001036163.1:p.Ile26Ser