Canonical Allele Identifier: CA2579376006

Gene: SECISBP2

Linked Data

• gnomAD v4: 9-89348027-ATCTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.89348029_89348033del , CM000671.2:g.89348029_89348033del	GRCh38
NC_000009.11:g.91962944_91962948del , CM000671.1:g.91962944_91962948del	GRCh37
NC_000009.10:g.91152764_91152768del	NCBI36
NG_012177.1:g.34533_34537del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375807.8:c.1603-50_1603-46del MANE Select	ENSP00000364965.3:n.1603-50_1603-46del
ENST00000339901.8:c.1384-50_1384-46del	ENSP00000364959.3:n.1384-50_1384-46del
ENST00000375807.7:c.1603-50_1603-46del	ENSP00000364965.3:n.1603-50_1603-46del
ENST00000534113.6:c.1399-50_1399-46del	ENSP00000436650.2:n.1399-50_1399-46del
NM_001282688.1:c.1600-50_1600-46del	NP_001269617.1:n.1600-50_1600-46del
NM_001282689.1:c.1384-50_1384-46del	NP_001269618.1:n.1384-50_1384-46del
NM_001282690.1:c.1399-50_1399-46del	NP_001269619.1:n.1399-50_1399-46del
NM_024077.4:c.1603-50_1603-46del	NP_076982.3:n.1603-50_1603-46del
XM_005252196.2:c.1486-50_1486-46del	XP_005252253.1:n.1486-50_1486-46del
XM_005252202.2:c.706-50_706-46del	XP_005252259.1:n.706-50_706-46del
XM_006717282.2:c.1384-50_1384-46del	XP_006717345.1:n.1384-50_1384-46del
XM_011519000.1:c.1399-50_1399-46del	XP_011517302.1:n.1399-50_1399-46del
XM_011519001.1:c.1309-50_1309-46del	XP_011517303.1:n.1309-50_1309-46del
XM_011519002.1:c.1285-50_1285-46del	XP_011517304.1:n.1285-50_1285-46del
XM_011519003.1:c.1282-50_1282-46del	XP_011517305.1:n.1282-50_1282-46del
XR_929840.1:n.1761-50_1761-46del
XR_929841.1:n.1761-50_1761-46del
XR_929842.1:n.1761-50_1761-46del
XR_929843.1:n.1761-50_1761-46del
NM_001354696.1:c.1486-50_1486-46del	NP_001341625.1:n.1486-50_1486-46del
NM_001354697.1:c.1489-50_1489-46del	NP_001341626.1:n.1489-50_1489-46del
NM_001354698.1:c.1396-50_1396-46del	NP_001341627.1:n.1396-50_1396-46del
NM_001354702.1:c.718-50_718-46del	NP_001341631.1:n.718-50_718-46del
XM_011519000.2:c.1399-50_1399-46del	XP_011517302.1:n.1399-50_1399-46del
XM_017015122.2:c.1513-50_1513-46del	XP_016870611.1:n.1513-50_1513-46del
XM_024447666.1:c.1399-50_1399-46del	XP_024303434.1:n.1399-50_1399-46del
XM_024447667.1:c.1267-50_1267-46del	XP_024303435.1:n.1267-50_1267-46del
XM_024447668.1:c.706-50_706-46del	XP_024303436.1:n.706-50_706-46del
XM_024447669.1:c.706-50_706-46del	XP_024303437.1:n.706-50_706-46del
XR_001746376.1:n.1761-50_1761-46del
XR_001746377.1:n.1761-50_1761-46del
XR_001746378.1:n.1761-50_1761-46del
XR_002956807.1:n.1761-50_1761-46del
NM_001282688.2:c.1600-50_1600-46del	NP_001269617.1:n.1600-50_1600-46del
NM_001282689.2:c.1384-50_1384-46del	NP_001269618.1:n.1384-50_1384-46del
NM_001354696.2:c.1486-50_1486-46del	NP_001341625.1:n.1486-50_1486-46del
NM_001354697.2:c.1489-50_1489-46del	NP_001341626.1:n.1489-50_1489-46del
NM_001354698.2:c.1396-50_1396-46del	NP_001341627.1:n.1396-50_1396-46del
NM_001354702.2:c.718-50_718-46del	NP_001341631.1:n.718-50_718-46del
NM_024077.5:c.1603-50_1603-46del MANE Select	NP_076982.3:n.1603-50_1603-46del