Canonical Allele Identifier: CA489234636

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386584A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141438A>G , CM000677.2:g.28141438A>G	GRCh38
NC_000015.9:g.28386584A>G , CM000677.1:g.28386584A>G	GRCh37
NC_000015.8:g.26060179A>G	NCBI36
NG_016355.1:g.185712T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.12009T>C MANE Select	ENSP00000261609.8:p.Asp4003=
ENST00000650509.1:c.3720T>C	ENSP00000496936.1:p.Asp1240=
ENST00000261609.11:c.12009T>C	ENSP00000261609.7:p.Asp4003=
NM_004667.5:c.12009T>C	NP_004658.3:p.Asp4003=
XM_005268276.3:c.11895T>C	XP_005268333.1:p.Asp3965=
XM_005268277.3:c.11895T>C	XP_005268334.1:p.Asp3965=
XM_006720726.2:c.11994T>C	XP_006720789.1:p.Asp3998=
XM_006720727.2:c.11751T>C	XP_006720790.1:p.Asp3917=
XM_011522131.1:c.11526T>C	XP_011520433.1:p.Asp3842=
XM_011522132.1:c.9525T>C	XP_011520434.1:p.Asp3175=
XM_011522133.1:c.8754T>C	XP_011520435.1:p.Asp2918=
XM_011522134.1:c.6126T>C	XP_011520436.1:p.Asp2042=
XM_005268276.5:c.11895T>C	XP_005268333.1:p.Asp3965=
XM_006720726.3:c.11994T>C	XP_006720789.1:p.Asp3998=
XM_006720727.3:c.11751T>C	XP_006720790.1:p.Asp3917=
XM_017022695.1:c.11895T>C	XP_016878184.1:p.Asp3965=
XM_017022696.1:c.11895T>C	XP_016878185.1:p.Asp3965=
XM_017022697.1:c.5175T>C	XP_016878186.1:p.Asp1725=
XM_017022698.1:c.5175T>C	XP_016878187.1:p.Asp1725=
NM_004667.6:c.12009T>C MANE Select	NP_004658.3:p.Asp4003=