Canonical Allele Identifier: CA391381441

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386705C>G (hg19) ; chr15:g.28141559C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141559C>G , CM000677.2:g.28141559C>G	GRCh38
NC_000015.9:g.28386705C>G , CM000677.1:g.28386705C>G	GRCh37
NC_000015.8:g.26060300C>G	NCBI36
NG_016355.1:g.185591G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11888G>C MANE Select	ENSP00000261609.8:p.Gly3963Ala
ENST00000650509.1:c.3599G>C	ENSP00000496936.1:p.Gly1200Ala
ENST00000261609.11:c.11888G>C	ENSP00000261609.7:p.Gly3963Ala
NM_004667.5:c.11888G>C	NP_004658.3:p.Gly3963Ala
XM_005268276.3:c.11774G>C	XP_005268333.1:p.Gly3925Ala
XM_005268277.3:c.11774G>C	XP_005268334.1:p.Gly3925Ala
XM_006720726.2:c.11873G>C	XP_006720789.1:p.Gly3958Ala
XM_006720727.2:c.11630G>C	XP_006720790.1:p.Gly3877Ala
XM_011522131.1:c.11405G>C	XP_011520433.1:p.Gly3802Ala
XM_011522132.1:c.9404G>C	XP_011520434.1:p.Gly3135Ala
XM_011522133.1:c.8633G>C	XP_011520435.1:p.Gly2878Ala
XM_011522134.1:c.6005G>C	XP_011520436.1:p.Gly2002Ala
XM_005268276.5:c.11774G>C	XP_005268333.1:p.Gly3925Ala
XM_006720726.3:c.11873G>C	XP_006720789.1:p.Gly3958Ala
XM_006720727.3:c.11630G>C	XP_006720790.1:p.Gly3877Ala
XM_017022695.1:c.11774G>C	XP_016878184.1:p.Gly3925Ala
XM_017022696.1:c.11774G>C	XP_016878185.1:p.Gly3925Ala
XM_017022697.1:c.5054G>C	XP_016878186.1:p.Gly1685Ala
XM_017022698.1:c.5054G>C	XP_016878187.1:p.Gly1685Ala
NM_004667.6:c.11888G>C MANE Select	NP_004658.3:p.Gly3963Ala