Canonical Allele Identifier: CA391381455

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386709T>A (hg19) ; chr15:g.28141563T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141563T>A , CM000677.2:g.28141563T>A	GRCh38
NC_000015.9:g.28386709T>A , CM000677.1:g.28386709T>A	GRCh37
NC_000015.8:g.26060304T>A	NCBI36
NG_016355.1:g.185587A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11884A>T MANE Select	ENSP00000261609.8:p.Arg3962Trp
ENST00000650509.1:c.3595A>T	ENSP00000496936.1:p.Arg1199Trp
ENST00000261609.11:c.11884A>T	ENSP00000261609.7:p.Arg3962Trp
NM_004667.5:c.11884A>T	NP_004658.3:p.Arg3962Trp
XM_005268276.3:c.11770A>T	XP_005268333.1:p.Arg3924Trp
XM_005268277.3:c.11770A>T	XP_005268334.1:p.Arg3924Trp
XM_006720726.2:c.11869A>T	XP_006720789.1:p.Arg3957Trp
XM_006720727.2:c.11626A>T	XP_006720790.1:p.Arg3876Trp
XM_011522131.1:c.11401A>T	XP_011520433.1:p.Arg3801Trp
XM_011522132.1:c.9400A>T	XP_011520434.1:p.Arg3134Trp
XM_011522133.1:c.8629A>T	XP_011520435.1:p.Arg2877Trp
XM_011522134.1:c.6001A>T	XP_011520436.1:p.Arg2001Trp
XM_005268276.5:c.11770A>T	XP_005268333.1:p.Arg3924Trp
XM_006720726.3:c.11869A>T	XP_006720789.1:p.Arg3957Trp
XM_006720727.3:c.11626A>T	XP_006720790.1:p.Arg3876Trp
XM_017022695.1:c.11770A>T	XP_016878184.1:p.Arg3924Trp
XM_017022696.1:c.11770A>T	XP_016878185.1:p.Arg3924Trp
XM_017022697.1:c.5050A>T	XP_016878186.1:p.Arg1684Trp
XM_017022698.1:c.5050A>T	XP_016878187.1:p.Arg1684Trp
NM_004667.6:c.11884A>T MANE Select	NP_004658.3:p.Arg3962Trp