Canonical Allele Identifier: CA391381585

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386738C>T (hg19) ; chr15:g.28141592C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141592C>T , CM000677.2:g.28141592C>T	GRCh38
NC_000015.9:g.28386738C>T , CM000677.1:g.28386738C>T	GRCh37
NC_000015.8:g.26060333C>T	NCBI36
NG_016355.1:g.185558G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11855G>A MANE Select	ENSP00000261609.8:p.Gly3952Glu
ENST00000650509.1:c.3566G>A	ENSP00000496936.1:p.Gly1189Glu
ENST00000261609.11:c.11855G>A	ENSP00000261609.7:p.Gly3952Glu
NM_004667.5:c.11855G>A	NP_004658.3:p.Gly3952Glu
XM_005268276.3:c.11741G>A	XP_005268333.1:p.Gly3914Glu
XM_005268277.3:c.11741G>A	XP_005268334.1:p.Gly3914Glu
XM_006720726.2:c.11840G>A	XP_006720789.1:p.Gly3947Glu
XM_006720727.2:c.11597G>A	XP_006720790.1:p.Gly3866Glu
XM_011522131.1:c.11372G>A	XP_011520433.1:p.Gly3791Glu
XM_011522132.1:c.9371G>A	XP_011520434.1:p.Gly3124Glu
XM_011522133.1:c.8600G>A	XP_011520435.1:p.Gly2867Glu
XM_011522134.1:c.5972G>A	XP_011520436.1:p.Gly1991Glu
XM_005268276.5:c.11741G>A	XP_005268333.1:p.Gly3914Glu
XM_006720726.3:c.11840G>A	XP_006720789.1:p.Gly3947Glu
XM_006720727.3:c.11597G>A	XP_006720790.1:p.Gly3866Glu
XM_017022695.1:c.11741G>A	XP_016878184.1:p.Gly3914Glu
XM_017022696.1:c.11741G>A	XP_016878185.1:p.Gly3914Glu
XM_017022697.1:c.5021G>A	XP_016878186.1:p.Gly1674Glu
XM_017022698.1:c.5021G>A	XP_016878187.1:p.Gly1674Glu
NM_004667.6:c.11855G>A MANE Select	NP_004658.3:p.Gly3952Glu