Canonical Allele Identifier: CA391380879

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386592T>A (hg19) ; chr15:g.28141446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141446T>A , CM000677.2:g.28141446T>A	GRCh38
NC_000015.9:g.28386592T>A , CM000677.1:g.28386592T>A	GRCh37
NC_000015.8:g.26060187T>A	NCBI36
NG_016355.1:g.185704A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.12001A>T MANE Select	ENSP00000261609.8:p.Thr4001Ser
ENST00000650509.1:c.3712A>T	ENSP00000496936.1:p.Thr1238Ser
ENST00000261609.11:c.12001A>T	ENSP00000261609.7:p.Thr4001Ser
NM_004667.5:c.12001A>T	NP_004658.3:p.Thr4001Ser
XM_005268276.3:c.11887A>T	XP_005268333.1:p.Thr3963Ser
XM_005268277.3:c.11887A>T	XP_005268334.1:p.Thr3963Ser
XM_006720726.2:c.11986A>T	XP_006720789.1:p.Thr3996Ser
XM_006720727.2:c.11743A>T	XP_006720790.1:p.Thr3915Ser
XM_011522131.1:c.11518A>T	XP_011520433.1:p.Thr3840Ser
XM_011522132.1:c.9517A>T	XP_011520434.1:p.Thr3173Ser
XM_011522133.1:c.8746A>T	XP_011520435.1:p.Thr2916Ser
XM_011522134.1:c.6118A>T	XP_011520436.1:p.Thr2040Ser
XM_005268276.5:c.11887A>T	XP_005268333.1:p.Thr3963Ser
XM_006720726.3:c.11986A>T	XP_006720789.1:p.Thr3996Ser
XM_006720727.3:c.11743A>T	XP_006720790.1:p.Thr3915Ser
XM_017022695.1:c.11887A>T	XP_016878184.1:p.Thr3963Ser
XM_017022696.1:c.11887A>T	XP_016878185.1:p.Thr3963Ser
XM_017022697.1:c.5167A>T	XP_016878186.1:p.Thr1723Ser
XM_017022698.1:c.5167A>T	XP_016878187.1:p.Thr1723Ser
NM_004667.6:c.12001A>T MANE Select	NP_004658.3:p.Thr4001Ser