Canonical Allele Identifier: CA391381473

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386712G>T (hg19) ; chr15:g.28141566G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141566G>T , CM000677.2:g.28141566G>T	GRCh38
NC_000015.9:g.28386712G>T , CM000677.1:g.28386712G>T	GRCh37
NC_000015.8:g.26060307G>T	NCBI36
NG_016355.1:g.185584C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11881C>A MANE Select	ENSP00000261609.8:p.His3961Asn
ENST00000650509.1:c.3592C>A	ENSP00000496936.1:p.His1198Asn
ENST00000261609.11:c.11881C>A	ENSP00000261609.7:p.His3961Asn
NM_004667.5:c.11881C>A	NP_004658.3:p.His3961Asn
XM_005268276.3:c.11767C>A	XP_005268333.1:p.His3923Asn
XM_005268277.3:c.11767C>A	XP_005268334.1:p.His3923Asn
XM_006720726.2:c.11866C>A	XP_006720789.1:p.His3956Asn
XM_006720727.2:c.11623C>A	XP_006720790.1:p.His3875Asn
XM_011522131.1:c.11398C>A	XP_011520433.1:p.His3800Asn
XM_011522132.1:c.9397C>A	XP_011520434.1:p.His3133Asn
XM_011522133.1:c.8626C>A	XP_011520435.1:p.His2876Asn
XM_011522134.1:c.5998C>A	XP_011520436.1:p.His2000Asn
XM_005268276.5:c.11767C>A	XP_005268333.1:p.His3923Asn
XM_006720726.3:c.11866C>A	XP_006720789.1:p.His3956Asn
XM_006720727.3:c.11623C>A	XP_006720790.1:p.His3875Asn
XM_017022695.1:c.11767C>A	XP_016878184.1:p.His3923Asn
XM_017022696.1:c.11767C>A	XP_016878185.1:p.His3923Asn
XM_017022697.1:c.5047C>A	XP_016878186.1:p.His1683Asn
XM_017022698.1:c.5047C>A	XP_016878187.1:p.His1683Asn
NM_004667.6:c.11881C>A MANE Select	NP_004658.3:p.His3961Asn