Canonical Allele Identifier: CA489234902

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386746A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141600A>T , CM000677.2:g.28141600A>T	GRCh38
NC_000015.9:g.28386746A>T , CM000677.1:g.28386746A>T	GRCh37
NC_000015.8:g.26060341A>T	NCBI36
NG_016355.1:g.185550T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11847T>A MANE Select	ENSP00000261609.8:p.Gly3949=
ENST00000650509.1:c.3558T>A	ENSP00000496936.1:p.Gly1186=
ENST00000261609.11:c.11847T>A	ENSP00000261609.7:p.Gly3949=
NM_004667.5:c.11847T>A	NP_004658.3:p.Gly3949=
XM_005268276.3:c.11733T>A	XP_005268333.1:p.Gly3911=
XM_005268277.3:c.11733T>A	XP_005268334.1:p.Gly3911=
XM_006720726.2:c.11832T>A	XP_006720789.1:p.Gly3944=
XM_006720727.2:c.11589T>A	XP_006720790.1:p.Gly3863=
XM_011522131.1:c.11364T>A	XP_011520433.1:p.Gly3788=
XM_011522132.1:c.9363T>A	XP_011520434.1:p.Gly3121=
XM_011522133.1:c.8592T>A	XP_011520435.1:p.Gly2864=
XM_011522134.1:c.5964T>A	XP_011520436.1:p.Gly1988=
XM_005268276.5:c.11733T>A	XP_005268333.1:p.Gly3911=
XM_006720726.3:c.11832T>A	XP_006720789.1:p.Gly3944=
XM_006720727.3:c.11589T>A	XP_006720790.1:p.Gly3863=
XM_017022695.1:c.11733T>A	XP_016878184.1:p.Gly3911=
XM_017022696.1:c.11733T>A	XP_016878185.1:p.Gly3911=
XM_017022697.1:c.5013T>A	XP_016878186.1:p.Gly1671=
XM_017022698.1:c.5013T>A	XP_016878187.1:p.Gly1671=
NM_004667.6:c.11847T>A MANE Select	NP_004658.3:p.Gly3949=