Canonical Allele Identifier: CA398376151

Gene: ZSWIM7

Linked Data

• MyVariant Identifiers: chr17:g.15890681G>T (hg19) ; chr17:g.15987367G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15987367G>T , CM000679.2:g.15987367G>T	GRCh38
NC_000017.10:g.15890681G>T , CM000679.1:g.15890681G>T	GRCh37
NC_000017.9:g.15831406G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399277.6:c.100C>A MANE Select	ENSP00000382218.1:p.Leu34Met
ENST00000399277.5:c.100C>A	ENSP00000382218.1:p.Leu34Met
ENST00000399280.6:n.59C>A
ENST00000460252.5:c.*17C>A	ENSP00000464463.1:n.*17C>A
ENST00000460315.5:c.*17C>A	ENSP00000462590.1:n.*17C>A
ENST00000472495.5:c.100C>A	ENSP00000419138.1:p.Leu34Met
ENST00000474716.5:c.*17C>A	ENSP00000464500.1:n.*17C>A
ENST00000475498.5:n.76C>A
ENST00000476496.5:c.110C>A	ENSP00000462208.1:n.110C>A
ENST00000486655.5:c.55C>A	ENSP00000464371.1:p.Leu19Met
ENST00000486706.6:c.*17C>A	ENSP00000463327.1:n.*17C>A
ENST00000490395.5:c.*17C>A	ENSP00000464605.1:n.*17C>A
ENST00000491631.5:c.*17C>A	ENSP00000462598.1:n.*17C>A
ENST00000495825.6:n.48C>A
ENST00000497719.5:n.78C>A
ENST00000579955.1:c.91C>A	ENSP00000463444.1:p.Leu31Met
ENST00000584519.5:c.78C>A	ENSP00000463592.1:p.Ser26Arg
ENST00000585208.5:c.*257C>A	ENSP00000464227.1:n.*257C>A
NM_001042697.1:c.100C>A	NP_001036162.1:p.Leu34Met
NM_001042698.1:c.100C>A	NP_001036163.1:p.Leu34Met
NM_001042697.2:c.100C>A MANE Select	NP_001036162.1:p.Leu34Met
NM_001042698.2:c.100C>A	NP_001036163.1:p.Leu34Met