Canonical Allele Identifier: CA516568618

Gene: SHROOM4

Linked Data

• MyVariant Identifiers: chrX:g.50378545A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50635545A>T , CM000685.2:g.50635545A>T	GRCh38
NC_000023.10:g.50378545A>T , CM000685.1:g.50378545A>T	GRCh37
NC_000023.9:g.50395285A>T	NCBI36
NG_011882.1:g.183500T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376020.9:c.528T>A MANE Select	ENSP00000365188.2:p.Pro176=
ENST00000376020.8:c.528T>A	ENSP00000365188.2:p.Pro176=
ENST00000289292.11:c.528T>A	ENSP00000289292.7:p.Pro176=
ENST00000376020.6:c.528T>A	ENSP00000365188.2:p.Pro176=
ENST00000460112.3:c.180T>A	ENSP00000421450.1:p.Pro60=
NM_020717.3:c.528T>A	NP_065768.2:p.Pro176=
NR_027121.1:n.554T>A
XM_006724590.2:c.180T>A	XP_006724653.1:p.Pro60=
XM_006724591.2:c.54T>A	XP_006724654.1:p.Pro18=
XM_011530800.1:c.393T>A	XP_011529102.1:p.Pro131=
XM_011530801.1:c.528T>A	XP_011529103.1:p.Pro176=
XR_938367.1:n.646T>A
XR_938368.1:n.646T>A
XM_017029682.2:c.528T>A	XP_016885171.1:p.Pro176=
XM_017029683.1:c.393T>A	XP_016885172.1:p.Pro131=
XM_017029684.1:c.180T>A	XP_016885173.1:p.Pro60=
XM_017029685.2:c.528T>A	XP_016885174.1:p.Pro176=
XM_017029686.1:c.54T>A	XP_016885175.1:p.Pro18=
XM_017029687.2:c.528T>A	XP_016885176.1:p.Pro176=
XR_001755716.2:n.659T>A
XR_001755717.2:n.659T>A
XR_001755718.2:n.659T>A
NM_020717.5:c.528T>A MANE Select	NP_065768.2:p.Pro176=
NR_027121.3:n.704T>A
NR_172068.1:n.569T>A
NR_172069.1:n.624T>A
NR_172070.1:n.489T>A