Canonical Allele Identifier: CA391381499

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386717T>A (hg19) ; chr15:g.28141571T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141571T>A , CM000677.2:g.28141571T>A	GRCh38
NC_000015.9:g.28386717T>A , CM000677.1:g.28386717T>A	GRCh37
NC_000015.8:g.26060312T>A	NCBI36
NG_016355.1:g.185579A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11876A>T MANE Select	ENSP00000261609.8:p.His3959Leu
ENST00000650509.1:c.3587A>T	ENSP00000496936.1:p.His1196Leu
ENST00000261609.11:c.11876A>T	ENSP00000261609.7:p.His3959Leu
NM_004667.5:c.11876A>T	NP_004658.3:p.His3959Leu
XM_005268276.3:c.11762A>T	XP_005268333.1:p.His3921Leu
XM_005268277.3:c.11762A>T	XP_005268334.1:p.His3921Leu
XM_006720726.2:c.11861A>T	XP_006720789.1:p.His3954Leu
XM_006720727.2:c.11618A>T	XP_006720790.1:p.His3873Leu
XM_011522131.1:c.11393A>T	XP_011520433.1:p.His3798Leu
XM_011522132.1:c.9392A>T	XP_011520434.1:p.His3131Leu
XM_011522133.1:c.8621A>T	XP_011520435.1:p.His2874Leu
XM_011522134.1:c.5993A>T	XP_011520436.1:p.His1998Leu
XM_005268276.5:c.11762A>T	XP_005268333.1:p.His3921Leu
XM_006720726.3:c.11861A>T	XP_006720789.1:p.His3954Leu
XM_006720727.3:c.11618A>T	XP_006720790.1:p.His3873Leu
XM_017022695.1:c.11762A>T	XP_016878184.1:p.His3921Leu
XM_017022696.1:c.11762A>T	XP_016878185.1:p.His3921Leu
XM_017022697.1:c.5042A>T	XP_016878186.1:p.His1681Leu
XM_017022698.1:c.5042A>T	XP_016878187.1:p.His1681Leu
NM_004667.6:c.11876A>T MANE Select	NP_004658.3:p.His3959Leu