Canonical Allele Identifier: CA1862787799
Gene: SECISBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.89348006G= , CM000671.2:g.89348006G= GRCh38
NC_000009.11:g.91962921G= , CM000671.1:g.91962921G= GRCh37
NC_000009.10:g.91152741G= NCBI36
NG_012177.1:g.34510G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375807.8:c.1603-73G= MANE Select ENSP00000364965.3:n.1603-73G=
ENST00000339901.8:c.1384-73G= ENSP00000364959.3:n.1384-73G=
ENST00000375807.7:c.1603-73G= ENSP00000364965.3:n.1603-73G=
ENST00000534113.6:c.1399-73G= ENSP00000436650.2:n.1399-73G=
NM_001282688.1:c.1600-73G= NP_001269617.1:n.1600-73G=
NM_001282689.1:c.1384-73G= NP_001269618.1:n.1384-73G=
NM_001282690.1:c.1399-73G= NP_001269619.1:n.1399-73G=
NM_024077.4:c.1603-73G= NP_076982.3:n.1603-73G=
XM_005252196.2:c.1486-73G= XP_005252253.1:n.1486-73G=
XM_005252202.2:c.706-73G= XP_005252259.1:n.706-73G=
XM_006717282.2:c.1384-73G= XP_006717345.1:n.1384-73G=
XM_011519000.1:c.1399-73G= XP_011517302.1:n.1399-73G=
XM_011519001.1:c.1309-73G= XP_011517303.1:n.1309-73G=
XM_011519002.1:c.1285-73G= XP_011517304.1:n.1285-73G=
XM_011519003.1:c.1282-73G= XP_011517305.1:n.1282-73G=
XR_929840.1:n.1761-73G=
XR_929841.1:n.1761-73G=
XR_929842.1:n.1761-73G=
XR_929843.1:n.1761-73G=
NM_001354696.1:c.1486-73G= NP_001341625.1:n.1486-73G=
NM_001354697.1:c.1489-73G= NP_001341626.1:n.1489-73G=
NM_001354698.1:c.1396-73G= NP_001341627.1:n.1396-73G=
NM_001354702.1:c.718-73G= NP_001341631.1:n.718-73G=
XM_011519000.2:c.1399-73G= XP_011517302.1:n.1399-73G=
XM_017015122.2:c.1513-73G= XP_016870611.1:n.1513-73G=
XM_024447666.1:c.1399-73G= XP_024303434.1:n.1399-73G=
XM_024447667.1:c.1267-73G= XP_024303435.1:n.1267-73G=
XM_024447668.1:c.706-73G= XP_024303436.1:n.706-73G=
XM_024447669.1:c.706-73G= XP_024303437.1:n.706-73G=
XR_001746376.1:n.1761-73G=
XR_001746377.1:n.1761-73G=
XR_001746378.1:n.1761-73G=
XR_002956807.1:n.1761-73G=
NM_001282688.2:c.1600-73G= NP_001269617.1:n.1600-73G=
NM_001282689.2:c.1384-73G= NP_001269618.1:n.1384-73G=
NM_001354696.2:c.1486-73G= NP_001341625.1:n.1486-73G=
NM_001354697.2:c.1489-73G= NP_001341626.1:n.1489-73G=
NM_001354698.2:c.1396-73G= NP_001341627.1:n.1396-73G=
NM_001354702.2:c.718-73G= NP_001341631.1:n.718-73G=
NM_024077.5:c.1603-73G= MANE Select NP_076982.3:n.1603-73G=