Canonical Allele Identifier: CA507317384

Gene: SYNE4

Linked Data

• MyVariant Identifiers: chr19:g.36497556G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36006654G>A , CM000681.2:g.36006654G>A	GRCh38
NC_000019.9:g.36497556G>A , CM000681.1:g.36497556G>A	GRCh37
NC_000019.8:g.41189396G>A	NCBI36
NG_042831.1:g.7140C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324444.9:c.636C>T MANE Select	ENSP00000316130.3:p.Asn212=
ENST00000397428.8:c.67-1217C>T
ENST00000465425.2:n.748C>T
ENST00000324444.7:c.636C>T	ENSP00000316130.3:p.Asn212=
ENST00000340477.9:c.297C>T	ENSP00000343152.5:p.Asn99=
ENST00000397428.7:c.40-1217C>T	ENSP00000380572.3:n.40-1217C>T
ENST00000465425.1:n.748C>T
ENST00000490730.1:c.636C>T	ENSP00000422716.1:p.Asn212=
ENST00000503121.5:c.242+1563C>T
ENST00000505054.2:n.395-1217C>T
NM_001039876.1:c.636C>T	NP_001034965.1:p.Asn212=
NM_001039876.2:c.636C>T	NP_001034965.1:p.Asn212=
NM_001297735.1:c.297C>T	NP_001284664.1:p.Asn99=
NM_001297735.2:c.297C>T	NP_001284664.1:p.Asn99=
XM_005258598.2:c.636C>T	XP_005258655.1:p.Asn212=
XM_005258601.2:c.618+96C>T	XP_005258658.1:n.618+96C>T
XM_005258604.3:c.636C>T	XP_005258661.1:p.Asn212=
NM_001039876.3:c.636C>T MANE Select	NP_001034965.1:p.Asn212=
NM_001297735.3:c.297C>T	NP_001284664.1:p.Asn99=