Canonical Allele Identifier: CA413126986

Gene: SHROOM4

Linked Data

• MyVariant Identifiers: chrX:g.50378645G>T (hg19) ; chrX:g.50635645G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.50635645G>T , CM000685.2:g.50635645G>T	GRCh38
NC_000023.10:g.50378645G>T , CM000685.1:g.50378645G>T	GRCh37
NC_000023.9:g.50395385G>T	NCBI36
NG_011882.1:g.183400C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376020.9:c.428C>A MANE Select	ENSP00000365188.2:p.Pro143Gln
ENST00000376020.8:c.428C>A	ENSP00000365188.2:p.Pro143Gln
ENST00000289292.11:c.428C>A	ENSP00000289292.7:p.Pro143Gln
ENST00000376020.6:c.428C>A	ENSP00000365188.2:p.Pro143Gln
ENST00000460112.3:c.80C>A	ENSP00000421450.1:p.Pro27Gln
NM_020717.3:c.428C>A	NP_065768.2:p.Pro143Gln
NR_027121.1:n.454C>A
XM_006724590.2:c.80C>A	XP_006724653.1:p.Pro27Gln
XM_006724591.2:c.-47C>A	XP_006724654.1:n.-47C>A
XM_011530800.1:c.293C>A	XP_011529102.1:p.Pro98Gln
XM_011530801.1:c.428C>A	XP_011529103.1:p.Pro143Gln
XR_938367.1:n.546C>A
XR_938368.1:n.546C>A
XM_017029682.2:c.428C>A	XP_016885171.1:p.Pro143Gln
XM_017029683.1:c.293C>A	XP_016885172.1:p.Pro98Gln
XM_017029684.1:c.80C>A	XP_016885173.1:p.Pro27Gln
XM_017029685.2:c.428C>A	XP_016885174.1:p.Pro143Gln
XM_017029686.1:c.-47C>A	XP_016885175.1:n.-47C>A
XM_017029687.2:c.428C>A	XP_016885176.1:p.Pro143Gln
XR_001755716.2:n.559C>A
XR_001755717.2:n.559C>A
XR_001755718.2:n.559C>A
NM_020717.5:c.428C>A MANE Select	NP_065768.2:p.Pro143Gln
NR_027121.3:n.604C>A
NR_172068.1:n.469C>A
NR_172069.1:n.524C>A
NR_172070.1:n.389C>A