Canonical Allele Identifier: CA391381802

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386883A>G (hg19) ; chr15:g.28141737A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141737A>G , CM000677.2:g.28141737A>G	GRCh38
NC_000015.9:g.28386883A>G , CM000677.1:g.28386883A>G	GRCh37
NC_000015.8:g.26060478A>G	NCBI36
NG_016355.1:g.185413T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11810T>C MANE Select	ENSP00000261609.8:p.Met3937Thr
ENST00000650509.1:c.3521T>C	ENSP00000496936.1:p.Met1174Thr
ENST00000261609.11:c.11810T>C	ENSP00000261609.7:p.Met3937Thr
NM_004667.5:c.11810T>C	NP_004658.3:p.Met3937Thr
XM_005268276.3:c.11696T>C	XP_005268333.1:p.Met3899Thr
XM_005268277.3:c.11696T>C	XP_005268334.1:p.Met3899Thr
XM_006720726.2:c.11795T>C	XP_006720789.1:p.Met3932Thr
XM_006720727.2:c.11552T>C	XP_006720790.1:p.Met3851Thr
XM_011522131.1:c.11327T>C	XP_011520433.1:p.Met3776Thr
XM_011522132.1:c.9326T>C	XP_011520434.1:p.Met3109Thr
XM_011522133.1:c.8555T>C	XP_011520435.1:p.Met2852Thr
XM_011522134.1:c.5927T>C	XP_011520436.1:p.Met1976Thr
XM_005268276.5:c.11696T>C	XP_005268333.1:p.Met3899Thr
XM_006720726.3:c.11795T>C	XP_006720789.1:p.Met3932Thr
XM_006720727.3:c.11552T>C	XP_006720790.1:p.Met3851Thr
XM_017022695.1:c.11696T>C	XP_016878184.1:p.Met3899Thr
XM_017022696.1:c.11696T>C	XP_016878185.1:p.Met3899Thr
XM_017022697.1:c.4976T>C	XP_016878186.1:p.Met1659Thr
XM_017022698.1:c.4976T>C	XP_016878187.1:p.Met1659Thr
NM_004667.6:c.11810T>C MANE Select	NP_004658.3:p.Met3937Thr