Canonical Allele Identifier: CA391381379

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386688C>A (hg19) ; chr15:g.28141542C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141542C>A , CM000677.2:g.28141542C>A	GRCh38
NC_000015.9:g.28386688C>A , CM000677.1:g.28386688C>A	GRCh37
NC_000015.8:g.26060283C>A	NCBI36
NG_016355.1:g.185608G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11905G>T MANE Select	ENSP00000261609.8:p.Glu3969Ter
ENST00000650509.1:c.3616G>T	ENSP00000496936.1:p.Glu1206Ter
ENST00000261609.11:c.11905G>T	ENSP00000261609.7:p.Glu3969Ter
NM_004667.5:c.11905G>T	NP_004658.3:p.Glu3969Ter
XM_005268276.3:c.11791G>T	XP_005268333.1:p.Glu3931Ter
XM_005268277.3:c.11791G>T	XP_005268334.1:p.Glu3931Ter
XM_006720726.2:c.11890G>T	XP_006720789.1:p.Glu3964Ter
XM_006720727.2:c.11647G>T	XP_006720790.1:p.Glu3883Ter
XM_011522131.1:c.11422G>T	XP_011520433.1:p.Glu3808Ter
XM_011522132.1:c.9421G>T	XP_011520434.1:p.Glu3141Ter
XM_011522133.1:c.8650G>T	XP_011520435.1:p.Glu2884Ter
XM_011522134.1:c.6022G>T	XP_011520436.1:p.Glu2008Ter
XM_005268276.5:c.11791G>T	XP_005268333.1:p.Glu3931Ter
XM_006720726.3:c.11890G>T	XP_006720789.1:p.Glu3964Ter
XM_006720727.3:c.11647G>T	XP_006720790.1:p.Glu3883Ter
XM_017022695.1:c.11791G>T	XP_016878184.1:p.Glu3931Ter
XM_017022696.1:c.11791G>T	XP_016878185.1:p.Glu3931Ter
XM_017022697.1:c.5071G>T	XP_016878186.1:p.Glu1691Ter
XM_017022698.1:c.5071G>T	XP_016878187.1:p.Glu1691Ter
NM_004667.6:c.11905G>T MANE Select	NP_004658.3:p.Glu3969Ter