Canonical Allele Identifier: CA1605368754

Gene: HUS1B EXOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.656415C= , CM000668.2:g.656415C=	GRCh38
NC_000006.11:g.656415C= , CM000668.1:g.656415C=	GRCh37
NC_000006.10:g.601415C=	NCBI36
NG_047166.1:g.41727G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018303.6:c.-43-18554G= (EXOC2) MANE Select	NP_060773.3:n.-43-18554G=
NM_148959.4:c.530G= (HUS1B) MANE Select	NP_683762.2:p.Ser177=
ENST00000230449.9:c.-43-18554G= (EXOC2) MANE Select	ENSP00000230449.4:n.-43-18554G=
ENST00000380907.3:c.530G= (HUS1B) MANE Select	ENSP00000370293.2:p.Ser177=
NM_018303.5:c.-43-18554G= (EXOC2)	NP_060773.3:n.-43-18554G=
NM_148959.3:c.530G= (HUS1B)	NP_683762.2:p.Ser177=
NR_073064.1:n.285+748G= (EXOC2)
NR_073064.2:n.283+748G= (EXOC2)
ENST00000230449.8:c.-43-18554G= (EXOC2)	ENSP00000230449.4:n.-43-18554G=
ENST00000380907.2:c.530G= (HUS1B)	ENSP00000370293.2:p.Ser177=
ENST00000443083.5:c.-44+748G= (EXOC2)	ENSP00000406400.1:n.-44+748G=
XM_017011018.1:c.-43-18554G= (EXOC2)	XP_016866507.1:n.-43-18554G=
XM_017011019.1:c.-43-18554G= (EXOC2)	XP_016866508.1:n.-43-18554G=
XM_017011020.1:c.-44+748G= (EXOC2)	XP_016866509.1:n.-44+748G=
XM_017011022.1:c.-43-18554G= (EXOC2)	XP_016866511.1:n.-43-18554G=
XM_017011023.1:c.-43-18554G= (EXOC2)	XP_016866512.1:n.-43-18554G=
XM_017011024.1:c.-43-18554G= (EXOC2)	XP_016866513.1:n.-43-18554G=
XM_017011025.1:c.-43-18554G= (EXOC2)	XP_016866514.1:n.-43-18554G=
XM_017011026.1:c.-43-18554G= (EXOC2)	XP_016866515.1:n.-43-18554G=