Canonical Allele Identifier: CA373989099

Gene: SECISBP2

Linked Data

• MyVariant Identifiers: chr9:g.91963013A>C (hg19) ; chr9:g.89348098A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.89348098A>C , CM000671.2:g.89348098A>C	GRCh38
NC_000009.11:g.91963013A>C , CM000671.1:g.91963013A>C	GRCh37
NC_000009.10:g.91152833A>C	NCBI36
NG_012177.1:g.34602A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375807.8:c.1622A>C MANE Select	ENSP00000364965.3:p.Gln541Pro
ENST00000339901.8:c.1403A>C	ENSP00000364959.3:p.Gln468Pro
ENST00000375807.7:c.1622A>C	ENSP00000364965.3:p.Gln541Pro
ENST00000534113.6:c.1418A>C	ENSP00000436650.2:p.Gln473Pro
NM_001282688.1:c.1619A>C	NP_001269617.1:p.Gln540Pro
NM_001282689.1:c.1403A>C	NP_001269618.1:p.Gln468Pro
NM_001282690.1:c.1418A>C	NP_001269619.1:p.Gln473Pro
NM_024077.4:c.1622A>C	NP_076982.3:p.Gln541Pro
XM_005252196.2:c.1505A>C	XP_005252253.1:p.Gln502Pro
XM_005252202.2:c.725A>C	XP_005252259.1:p.Gln242Pro
XM_006717282.2:c.1403A>C	XP_006717345.1:p.Gln468Pro
XM_011519000.1:c.1418A>C	XP_011517302.1:p.Gln473Pro
XM_011519001.1:c.1328A>C	XP_011517303.1:p.Gln443Pro
XM_011519002.1:c.1304A>C	XP_011517304.1:p.Gln435Pro
XM_011519003.1:c.1301A>C	XP_011517305.1:p.Gln434Pro
XR_929840.1:n.1780A>C
XR_929841.1:n.1780A>C
XR_929842.1:n.1780A>C
XR_929843.1:n.1780A>C
NM_001354696.1:c.1505A>C	NP_001341625.1:p.Gln502Pro
NM_001354697.1:c.1508A>C	NP_001341626.1:p.Gln503Pro
NM_001354698.1:c.1415A>C	NP_001341627.1:p.Gln472Pro
NM_001354702.1:c.737A>C	NP_001341631.1:p.Gln246Pro
XM_011519000.2:c.1418A>C	XP_011517302.1:p.Gln473Pro
XM_017015122.2:c.1532A>C	XP_016870611.1:p.Gln511Pro
XM_024447666.1:c.1418A>C	XP_024303434.1:p.Gln473Pro
XM_024447667.1:c.1286A>C	XP_024303435.1:p.Gln429Pro
XM_024447668.1:c.725A>C	XP_024303436.1:p.Gln242Pro
XM_024447669.1:c.725A>C	XP_024303437.1:p.Gln242Pro
XR_001746376.1:n.1780A>C
XR_001746377.1:n.1780A>C
XR_001746378.1:n.1780A>C
XR_002956807.1:n.1780A>C
NM_001282688.2:c.1619A>C	NP_001269617.1:p.Gln540Pro
NM_001282689.2:c.1403A>C	NP_001269618.1:p.Gln468Pro
NM_001354696.2:c.1505A>C	NP_001341625.1:p.Gln502Pro
NM_001354697.2:c.1508A>C	NP_001341626.1:p.Gln503Pro
NM_001354698.2:c.1415A>C	NP_001341627.1:p.Gln472Pro
NM_001354702.2:c.737A>C	NP_001341631.1:p.Gln246Pro
NM_024077.5:c.1622A>C MANE Select	NP_076982.3:p.Gln541Pro