Canonical Allele Identifier: CA488962634

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386987A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141841A>C , CM000677.2:g.28141841A>C	GRCh38
NC_000015.9:g.28386987A>C , CM000677.1:g.28386987A>C	GRCh37
NC_000015.8:g.26060582A>C	NCBI36
NG_016355.1:g.185309T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11706T>G MANE Select	ENSP00000261609.8:p.Ala3902=
ENST00000650509.1:c.3417T>G	ENSP00000496936.1:p.Ala1139=
ENST00000261609.11:c.11706T>G	ENSP00000261609.7:p.Ala3902=
ENST00000564519.1:n.221T>G
NM_004667.5:c.11706T>G	NP_004658.3:p.Ala3902=
XM_005268276.3:c.11592T>G	XP_005268333.1:p.Ala3864=
XM_005268277.3:c.11592T>G	XP_005268334.1:p.Ala3864=
XM_006720726.2:c.11691T>G	XP_006720789.1:p.Ala3897=
XM_006720727.2:c.11448T>G	XP_006720790.1:p.Ala3816=
XM_011522131.1:c.11223T>G	XP_011520433.1:p.Ala3741=
XM_011522132.1:c.9222T>G	XP_011520434.1:p.Ala3074=
XM_011522133.1:c.8451T>G	XP_011520435.1:p.Ala2817=
XM_011522134.1:c.5823T>G	XP_011520436.1:p.Ala1941=
XM_005268276.5:c.11592T>G	XP_005268333.1:p.Ala3864=
XM_006720726.3:c.11691T>G	XP_006720789.1:p.Ala3897=
XM_006720727.3:c.11448T>G	XP_006720790.1:p.Ala3816=
XM_017022695.1:c.11592T>G	XP_016878184.1:p.Ala3864=
XM_017022696.1:c.11592T>G	XP_016878185.1:p.Ala3864=
XM_017022697.1:c.4872T>G	XP_016878186.1:p.Ala1624=
XM_017022698.1:c.4872T>G	XP_016878187.1:p.Ala1624=
NM_004667.6:c.11706T>G MANE Select	NP_004658.3:p.Ala3902=