Canonical Allele Identifier: CA489234756

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386680T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141534T>C , CM000677.2:g.28141534T>C	GRCh38
NC_000015.9:g.28386680T>C , CM000677.1:g.28386680T>C	GRCh37
NC_000015.8:g.26060275T>C	NCBI36
NG_016355.1:g.185616A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11913A>G MANE Select	ENSP00000261609.8:p.Ala3971=
ENST00000650509.1:c.3624A>G	ENSP00000496936.1:p.Ala1208=
ENST00000261609.11:c.11913A>G	ENSP00000261609.7:p.Ala3971=
NM_004667.5:c.11913A>G	NP_004658.3:p.Ala3971=
XM_005268276.3:c.11799A>G	XP_005268333.1:p.Ala3933=
XM_005268277.3:c.11799A>G	XP_005268334.1:p.Ala3933=
XM_006720726.2:c.11898A>G	XP_006720789.1:p.Ala3966=
XM_006720727.2:c.11655A>G	XP_006720790.1:p.Ala3885=
XM_011522131.1:c.11430A>G	XP_011520433.1:p.Ala3810=
XM_011522132.1:c.9429A>G	XP_011520434.1:p.Ala3143=
XM_011522133.1:c.8658A>G	XP_011520435.1:p.Ala2886=
XM_011522134.1:c.6030A>G	XP_011520436.1:p.Ala2010=
XM_005268276.5:c.11799A>G	XP_005268333.1:p.Ala3933=
XM_006720726.3:c.11898A>G	XP_006720789.1:p.Ala3966=
XM_006720727.3:c.11655A>G	XP_006720790.1:p.Ala3885=
XM_017022695.1:c.11799A>G	XP_016878184.1:p.Ala3933=
XM_017022696.1:c.11799A>G	XP_016878185.1:p.Ala3933=
XM_017022697.1:c.5079A>G	XP_016878186.1:p.Ala1693=
XM_017022698.1:c.5079A>G	XP_016878187.1:p.Ala1693=
NM_004667.6:c.11913A>G MANE Select	NP_004658.3:p.Ala3971=