Canonical Allele Identifier: CA391381412

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386697C>A (hg19) ; chr15:g.28141551C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141551C>A , CM000677.2:g.28141551C>A	GRCh38
NC_000015.9:g.28386697C>A , CM000677.1:g.28386697C>A	GRCh37
NC_000015.8:g.26060292C>A	NCBI36
NG_016355.1:g.185599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11896G>T MANE Select	ENSP00000261609.8:p.Gly3966Trp
ENST00000650509.1:c.3607G>T	ENSP00000496936.1:p.Gly1203Trp
ENST00000261609.11:c.11896G>T	ENSP00000261609.7:p.Gly3966Trp
NM_004667.5:c.11896G>T	NP_004658.3:p.Gly3966Trp
XM_005268276.3:c.11782G>T	XP_005268333.1:p.Gly3928Trp
XM_005268277.3:c.11782G>T	XP_005268334.1:p.Gly3928Trp
XM_006720726.2:c.11881G>T	XP_006720789.1:p.Gly3961Trp
XM_006720727.2:c.11638G>T	XP_006720790.1:p.Gly3880Trp
XM_011522131.1:c.11413G>T	XP_011520433.1:p.Gly3805Trp
XM_011522132.1:c.9412G>T	XP_011520434.1:p.Gly3138Trp
XM_011522133.1:c.8641G>T	XP_011520435.1:p.Gly2881Trp
XM_011522134.1:c.6013G>T	XP_011520436.1:p.Gly2005Trp
XM_005268276.5:c.11782G>T	XP_005268333.1:p.Gly3928Trp
XM_006720726.3:c.11881G>T	XP_006720789.1:p.Gly3961Trp
XM_006720727.3:c.11638G>T	XP_006720790.1:p.Gly3880Trp
XM_017022695.1:c.11782G>T	XP_016878184.1:p.Gly3928Trp
XM_017022696.1:c.11782G>T	XP_016878185.1:p.Gly3928Trp
XM_017022697.1:c.5062G>T	XP_016878186.1:p.Gly1688Trp
XM_017022698.1:c.5062G>T	XP_016878187.1:p.Gly1688Trp
NM_004667.6:c.11896G>T MANE Select	NP_004658.3:p.Gly3966Trp