Canonical Allele Identifier: CA373989101

Gene: SECISBP2

Linked Data

• MyVariant Identifiers: chr9:g.91963014A>T (hg19) ; chr9:g.89348099A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.89348099A>T , CM000671.2:g.89348099A>T	GRCh38
NC_000009.11:g.91963014A>T , CM000671.1:g.91963014A>T	GRCh37
NC_000009.10:g.91152834A>T	NCBI36
NG_012177.1:g.34603A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375807.8:c.1623A>T MANE Select	ENSP00000364965.3:p.Gln541His
ENST00000339901.8:c.1404A>T	ENSP00000364959.3:p.Gln468His
ENST00000375807.7:c.1623A>T	ENSP00000364965.3:p.Gln541His
ENST00000534113.6:c.1419A>T	ENSP00000436650.2:p.Gln473His
NM_001282688.1:c.1620A>T	NP_001269617.1:p.Gln540His
NM_001282689.1:c.1404A>T	NP_001269618.1:p.Gln468His
NM_001282690.1:c.1419A>T	NP_001269619.1:p.Gln473His
NM_024077.4:c.1623A>T	NP_076982.3:p.Gln541His
XM_005252196.2:c.1506A>T	XP_005252253.1:p.Gln502His
XM_005252202.2:c.726A>T	XP_005252259.1:p.Gln242His
XM_006717282.2:c.1404A>T	XP_006717345.1:p.Gln468His
XM_011519000.1:c.1419A>T	XP_011517302.1:p.Gln473His
XM_011519001.1:c.1329A>T	XP_011517303.1:p.Gln443His
XM_011519002.1:c.1305A>T	XP_011517304.1:p.Gln435His
XM_011519003.1:c.1302A>T	XP_011517305.1:p.Gln434His
XR_929840.1:n.1781A>T
XR_929841.1:n.1781A>T
XR_929842.1:n.1781A>T
XR_929843.1:n.1781A>T
NM_001354696.1:c.1506A>T	NP_001341625.1:p.Gln502His
NM_001354697.1:c.1509A>T	NP_001341626.1:p.Gln503His
NM_001354698.1:c.1416A>T	NP_001341627.1:p.Gln472His
NM_001354702.1:c.738A>T	NP_001341631.1:p.Gln246His
XM_011519000.2:c.1419A>T	XP_011517302.1:p.Gln473His
XM_017015122.2:c.1533A>T	XP_016870611.1:p.Gln511His
XM_024447666.1:c.1419A>T	XP_024303434.1:p.Gln473His
XM_024447667.1:c.1287A>T	XP_024303435.1:p.Gln429His
XM_024447668.1:c.726A>T	XP_024303436.1:p.Gln242His
XM_024447669.1:c.726A>T	XP_024303437.1:p.Gln242His
XR_001746376.1:n.1781A>T
XR_001746377.1:n.1781A>T
XR_001746378.1:n.1781A>T
XR_002956807.1:n.1781A>T
NM_001282688.2:c.1620A>T	NP_001269617.1:p.Gln540His
NM_001282689.2:c.1404A>T	NP_001269618.1:p.Gln468His
NM_001354696.2:c.1506A>T	NP_001341625.1:p.Gln502His
NM_001354697.2:c.1509A>T	NP_001341626.1:p.Gln503His
NM_001354698.2:c.1416A>T	NP_001341627.1:p.Gln472His
NM_001354702.2:c.738A>T	NP_001341631.1:p.Gln246His
NM_024077.5:c.1623A>T MANE Select	NP_076982.3:p.Gln541His