Canonical Allele Identifier: CA391381803

Gene: HERC2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11810T>A MANE Select	ENSP00000261609.8:p.Met3937Lys
ENST00000650509.1:c.3521T>A	ENSP00000496936.1:p.Met1174Lys
ENST00000261609.11:c.11810T>A	ENSP00000261609.7:p.Met3937Lys
NM_004667.5:c.11810T>A	NP_004658.3:p.Met3937Lys
XM_005268276.3:c.11696T>A	XP_005268333.1:p.Met3899Lys
XM_005268277.3:c.11696T>A	XP_005268334.1:p.Met3899Lys
XM_006720726.2:c.11795T>A	XP_006720789.1:p.Met3932Lys
XM_006720727.2:c.11552T>A	XP_006720790.1:p.Met3851Lys
XM_011522131.1:c.11327T>A	XP_011520433.1:p.Met3776Lys
XM_011522132.1:c.9326T>A	XP_011520434.1:p.Met3109Lys
XM_011522133.1:c.8555T>A	XP_011520435.1:p.Met2852Lys
XM_011522134.1:c.5927T>A	XP_011520436.1:p.Met1976Lys
XM_005268276.5:c.11696T>A	XP_005268333.1:p.Met3899Lys
XM_006720726.3:c.11795T>A	XP_006720789.1:p.Met3932Lys
XM_006720727.3:c.11552T>A	XP_006720790.1:p.Met3851Lys
XM_017022695.1:c.11696T>A	XP_016878184.1:p.Met3899Lys
XM_017022696.1:c.11696T>A	XP_016878185.1:p.Met3899Lys
XM_017022697.1:c.4976T>A	XP_016878186.1:p.Met1659Lys
XM_017022698.1:c.4976T>A	XP_016878187.1:p.Met1659Lys
NM_004667.6:c.11810T>A MANE Select	NP_004658.3:p.Met3937Lys