Canonical Allele Identifier: CA391381513

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141574-C-A
• MyVariant Identifiers: chr15:g.28386720C>A (hg19) ; chr15:g.28141574C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141574C>A , CM000677.2:g.28141574C>A	GRCh38
NC_000015.9:g.28386720C>A , CM000677.1:g.28386720C>A	GRCh37
NC_000015.8:g.26060315C>A	NCBI36
NG_016355.1:g.185576G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11873G>T MANE Select	ENSP00000261609.8:p.Gly3958Val
ENST00000650509.1:c.3584G>T	ENSP00000496936.1:p.Gly1195Val
ENST00000261609.11:c.11873G>T	ENSP00000261609.7:p.Gly3958Val
NM_004667.5:c.11873G>T	NP_004658.3:p.Gly3958Val
XM_005268276.3:c.11759G>T	XP_005268333.1:p.Gly3920Val
XM_005268277.3:c.11759G>T	XP_005268334.1:p.Gly3920Val
XM_006720726.2:c.11858G>T	XP_006720789.1:p.Gly3953Val
XM_006720727.2:c.11615G>T	XP_006720790.1:p.Gly3872Val
XM_011522131.1:c.11390G>T	XP_011520433.1:p.Gly3797Val
XM_011522132.1:c.9389G>T	XP_011520434.1:p.Gly3130Val
XM_011522133.1:c.8618G>T	XP_011520435.1:p.Gly2873Val
XM_011522134.1:c.5990G>T	XP_011520436.1:p.Gly1997Val
XM_005268276.5:c.11759G>T	XP_005268333.1:p.Gly3920Val
XM_006720726.3:c.11858G>T	XP_006720789.1:p.Gly3953Val
XM_006720727.3:c.11615G>T	XP_006720790.1:p.Gly3872Val
XM_017022695.1:c.11759G>T	XP_016878184.1:p.Gly3920Val
XM_017022696.1:c.11759G>T	XP_016878185.1:p.Gly3920Val
XM_017022697.1:c.5039G>T	XP_016878186.1:p.Gly1680Val
XM_017022698.1:c.5039G>T	XP_016878187.1:p.Gly1680Val
NM_004667.6:c.11873G>T MANE Select	NP_004658.3:p.Gly3958Val