Canonical Allele Identifier: CA391381301

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386670C>A (hg19) ; chr15:g.28141524C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141524C>A , CM000677.2:g.28141524C>A	GRCh38
NC_000015.9:g.28386670C>A , CM000677.1:g.28386670C>A	GRCh37
NC_000015.8:g.26060265C>A	NCBI36
NG_016355.1:g.185626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11923G>T MANE Select	ENSP00000261609.8:p.Val3975Phe
ENST00000650509.1:c.3634G>T	ENSP00000496936.1:p.Val1212Phe
ENST00000261609.11:c.11923G>T	ENSP00000261609.7:p.Val3975Phe
NM_004667.5:c.11923G>T	NP_004658.3:p.Val3975Phe
XM_005268276.3:c.11809G>T	XP_005268333.1:p.Val3937Phe
XM_005268277.3:c.11809G>T	XP_005268334.1:p.Val3937Phe
XM_006720726.2:c.11908G>T	XP_006720789.1:p.Val3970Phe
XM_006720727.2:c.11665G>T	XP_006720790.1:p.Val3889Phe
XM_011522131.1:c.11440G>T	XP_011520433.1:p.Val3814Phe
XM_011522132.1:c.9439G>T	XP_011520434.1:p.Val3147Phe
XM_011522133.1:c.8668G>T	XP_011520435.1:p.Val2890Phe
XM_011522134.1:c.6040G>T	XP_011520436.1:p.Val2014Phe
XM_005268276.5:c.11809G>T	XP_005268333.1:p.Val3937Phe
XM_006720726.3:c.11908G>T	XP_006720789.1:p.Val3970Phe
XM_006720727.3:c.11665G>T	XP_006720790.1:p.Val3889Phe
XM_017022695.1:c.11809G>T	XP_016878184.1:p.Val3937Phe
XM_017022696.1:c.11809G>T	XP_016878185.1:p.Val3937Phe
XM_017022697.1:c.5089G>T	XP_016878186.1:p.Val1697Phe
XM_017022698.1:c.5089G>T	XP_016878187.1:p.Val1697Phe
NM_004667.6:c.11923G>T MANE Select	NP_004658.3:p.Val3975Phe