Canonical Allele Identifier: CA489234740

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386668A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141522A>T , CM000677.2:g.28141522A>T	GRCh38
NC_000015.9:g.28386668A>T , CM000677.1:g.28386668A>T	GRCh37
NC_000015.8:g.26060263A>T	NCBI36
NG_016355.1:g.185628T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11925T>A MANE Select	ENSP00000261609.8:p.Val3975=
ENST00000650509.1:c.3636T>A	ENSP00000496936.1:p.Val1212=
ENST00000261609.11:c.11925T>A	ENSP00000261609.7:p.Val3975=
NM_004667.5:c.11925T>A	NP_004658.3:p.Val3975=
XM_005268276.3:c.11811T>A	XP_005268333.1:p.Val3937=
XM_005268277.3:c.11811T>A	XP_005268334.1:p.Val3937=
XM_006720726.2:c.11910T>A	XP_006720789.1:p.Val3970=
XM_006720727.2:c.11667T>A	XP_006720790.1:p.Val3889=
XM_011522131.1:c.11442T>A	XP_011520433.1:p.Val3814=
XM_011522132.1:c.9441T>A	XP_011520434.1:p.Val3147=
XM_011522133.1:c.8670T>A	XP_011520435.1:p.Val2890=
XM_011522134.1:c.6042T>A	XP_011520436.1:p.Val2014=
XM_005268276.5:c.11811T>A	XP_005268333.1:p.Val3937=
XM_006720726.3:c.11910T>A	XP_006720789.1:p.Val3970=
XM_006720727.3:c.11667T>A	XP_006720790.1:p.Val3889=
XM_017022695.1:c.11811T>A	XP_016878184.1:p.Val3937=
XM_017022696.1:c.11811T>A	XP_016878185.1:p.Val3937=
XM_017022697.1:c.5091T>A	XP_016878186.1:p.Val1697=
XM_017022698.1:c.5091T>A	XP_016878187.1:p.Val1697=
NM_004667.6:c.11925T>A MANE Select	NP_004658.3:p.Val3975=