Canonical Allele Identifier: CA391381610

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386744C>T (hg19) ; chr15:g.28141598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141598C>T , CM000677.2:g.28141598C>T	GRCh38
NC_000015.9:g.28386744C>T , CM000677.1:g.28386744C>T	GRCh37
NC_000015.8:g.26060339C>T	NCBI36
NG_016355.1:g.185552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11849G>A MANE Select	ENSP00000261609.8:p.Gly3950Asp
ENST00000650509.1:c.3560G>A	ENSP00000496936.1:p.Gly1187Asp
ENST00000261609.11:c.11849G>A	ENSP00000261609.7:p.Gly3950Asp
NM_004667.5:c.11849G>A	NP_004658.3:p.Gly3950Asp
XM_005268276.3:c.11735G>A	XP_005268333.1:p.Gly3912Asp
XM_005268277.3:c.11735G>A	XP_005268334.1:p.Gly3912Asp
XM_006720726.2:c.11834G>A	XP_006720789.1:p.Gly3945Asp
XM_006720727.2:c.11591G>A	XP_006720790.1:p.Gly3864Asp
XM_011522131.1:c.11366G>A	XP_011520433.1:p.Gly3789Asp
XM_011522132.1:c.9365G>A	XP_011520434.1:p.Gly3122Asp
XM_011522133.1:c.8594G>A	XP_011520435.1:p.Gly2865Asp
XM_011522134.1:c.5966G>A	XP_011520436.1:p.Gly1989Asp
XM_005268276.5:c.11735G>A	XP_005268333.1:p.Gly3912Asp
XM_006720726.3:c.11834G>A	XP_006720789.1:p.Gly3945Asp
XM_006720727.3:c.11591G>A	XP_006720790.1:p.Gly3864Asp
XM_017022695.1:c.11735G>A	XP_016878184.1:p.Gly3912Asp
XM_017022696.1:c.11735G>A	XP_016878185.1:p.Gly3912Asp
XM_017022697.1:c.5015G>A	XP_016878186.1:p.Gly1672Asp
XM_017022698.1:c.5015G>A	XP_016878187.1:p.Gly1672Asp
NM_004667.6:c.11849G>A MANE Select	NP_004658.3:p.Gly3950Asp