Canonical Allele Identifier: CA391381283

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386663G>C (hg19) ; chr15:g.28141517G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141517G>C , CM000677.2:g.28141517G>C	GRCh38
NC_000015.9:g.28386663G>C , CM000677.1:g.28386663G>C	GRCh37
NC_000015.8:g.26060258G>C	NCBI36
NG_016355.1:g.185633C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11930C>G MANE Select	ENSP00000261609.8:p.Thr3977Ser
ENST00000650509.1:c.3641C>G	ENSP00000496936.1:p.Thr1214Ser
ENST00000261609.11:c.11930C>G	ENSP00000261609.7:p.Thr3977Ser
NM_004667.5:c.11930C>G	NP_004658.3:p.Thr3977Ser
XM_005268276.3:c.11816C>G	XP_005268333.1:p.Thr3939Ser
XM_005268277.3:c.11816C>G	XP_005268334.1:p.Thr3939Ser
XM_006720726.2:c.11915C>G	XP_006720789.1:p.Thr3972Ser
XM_006720727.2:c.11672C>G	XP_006720790.1:p.Thr3891Ser
XM_011522131.1:c.11447C>G	XP_011520433.1:p.Thr3816Ser
XM_011522132.1:c.9446C>G	XP_011520434.1:p.Thr3149Ser
XM_011522133.1:c.8675C>G	XP_011520435.1:p.Thr2892Ser
XM_011522134.1:c.6047C>G	XP_011520436.1:p.Thr2016Ser
XM_005268276.5:c.11816C>G	XP_005268333.1:p.Thr3939Ser
XM_006720726.3:c.11915C>G	XP_006720789.1:p.Thr3972Ser
XM_006720727.3:c.11672C>G	XP_006720790.1:p.Thr3891Ser
XM_017022695.1:c.11816C>G	XP_016878184.1:p.Thr3939Ser
XM_017022696.1:c.11816C>G	XP_016878185.1:p.Thr3939Ser
XM_017022697.1:c.5096C>G	XP_016878186.1:p.Thr1699Ser
XM_017022698.1:c.5096C>G	XP_016878187.1:p.Thr1699Ser
NM_004667.6:c.11930C>G MANE Select	NP_004658.3:p.Thr3977Ser