Canonical Allele Identifier: CA391382060

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141846-C-T
• MyVariant Identifiers: chr15:g.28386992C>T (hg19) ; chr15:g.28141846C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141846C>T , CM000677.2:g.28141846C>T	GRCh38
NC_000015.9:g.28386992C>T , CM000677.1:g.28386992C>T	GRCh37
NC_000015.8:g.26060587C>T	NCBI36
NG_016355.1:g.185304G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11701G>A MANE Select	ENSP00000261609.8:p.Val3901Met
ENST00000650509.1:c.3412G>A	ENSP00000496936.1:p.Val1138Met
ENST00000261609.11:c.11701G>A	ENSP00000261609.7:p.Val3901Met
ENST00000564519.1:n.216G>A
NM_004667.5:c.11701G>A	NP_004658.3:p.Val3901Met
XM_005268276.3:c.11587G>A	XP_005268333.1:p.Val3863Met
XM_005268277.3:c.11587G>A	XP_005268334.1:p.Val3863Met
XM_006720726.2:c.11686G>A	XP_006720789.1:p.Val3896Met
XM_006720727.2:c.11443G>A	XP_006720790.1:p.Val3815Met
XM_011522131.1:c.11218G>A	XP_011520433.1:p.Val3740Met
XM_011522132.1:c.9217G>A	XP_011520434.1:p.Val3073Met
XM_011522133.1:c.8446G>A	XP_011520435.1:p.Val2816Met
XM_011522134.1:c.5818G>A	XP_011520436.1:p.Val1940Met
XM_005268276.5:c.11587G>A	XP_005268333.1:p.Val3863Met
XM_006720726.3:c.11686G>A	XP_006720789.1:p.Val3896Met
XM_006720727.3:c.11443G>A	XP_006720790.1:p.Val3815Met
XM_017022695.1:c.11587G>A	XP_016878184.1:p.Val3863Met
XM_017022696.1:c.11587G>A	XP_016878185.1:p.Val3863Met
XM_017022697.1:c.4867G>A	XP_016878186.1:p.Val1623Met
XM_017022698.1:c.4867G>A	XP_016878187.1:p.Val1623Met
NM_004667.6:c.11701G>A MANE Select	NP_004658.3:p.Val3901Met