Canonical Allele Identifier: CA489235039

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386930G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141784G>A , CM000677.2:g.28141784G>A	GRCh38
NC_000015.9:g.28386930G>A , CM000677.1:g.28386930G>A	GRCh37
NC_000015.8:g.26060525G>A	NCBI36
NG_016355.1:g.185366C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11763C>T MANE Select	ENSP00000261609.8:p.Ser3921=
ENST00000650509.1:c.3474C>T	ENSP00000496936.1:p.Ser1158=
ENST00000261609.11:c.11763C>T	ENSP00000261609.7:p.Ser3921=
ENST00000564519.1:n.278C>T
NM_004667.5:c.11763C>T	NP_004658.3:p.Ser3921=
XM_005268276.3:c.11649C>T	XP_005268333.1:p.Ser3883=
XM_005268277.3:c.11649C>T	XP_005268334.1:p.Ser3883=
XM_006720726.2:c.11748C>T	XP_006720789.1:p.Ser3916=
XM_006720727.2:c.11505C>T	XP_006720790.1:p.Ser3835=
XM_011522131.1:c.11280C>T	XP_011520433.1:p.Ser3760=
XM_011522132.1:c.9279C>T	XP_011520434.1:p.Ser3093=
XM_011522133.1:c.8508C>T	XP_011520435.1:p.Ser2836=
XM_011522134.1:c.5880C>T	XP_011520436.1:p.Ser1960=
XM_005268276.5:c.11649C>T	XP_005268333.1:p.Ser3883=
XM_006720726.3:c.11748C>T	XP_006720789.1:p.Ser3916=
XM_006720727.3:c.11505C>T	XP_006720790.1:p.Ser3835=
XM_017022695.1:c.11649C>T	XP_016878184.1:p.Ser3883=
XM_017022696.1:c.11649C>T	XP_016878185.1:p.Ser3883=
XM_017022697.1:c.4929C>T	XP_016878186.1:p.Ser1643=
XM_017022698.1:c.4929C>T	XP_016878187.1:p.Ser1643=
NM_004667.6:c.11763C>T MANE Select	NP_004658.3:p.Ser3921=