Canonical Allele Identifier: CA391382009

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141822-T-C
• MyVariant Identifiers: chr15:g.28386968T>C (hg19) ; chr15:g.28141822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141822T>C , CM000677.2:g.28141822T>C	GRCh38
NC_000015.9:g.28386968T>C , CM000677.1:g.28386968T>C	GRCh37
NC_000015.8:g.26060563T>C	NCBI36
NG_016355.1:g.185328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11725A>G MANE Select	ENSP00000261609.8:p.Met3909Val
ENST00000650509.1:c.3436A>G	ENSP00000496936.1:p.Met1146Val
ENST00000261609.11:c.11725A>G	ENSP00000261609.7:p.Met3909Val
ENST00000564519.1:n.240A>G
NM_004667.5:c.11725A>G	NP_004658.3:p.Met3909Val
XM_005268276.3:c.11611A>G	XP_005268333.1:p.Met3871Val
XM_005268277.3:c.11611A>G	XP_005268334.1:p.Met3871Val
XM_006720726.2:c.11710A>G	XP_006720789.1:p.Met3904Val
XM_006720727.2:c.11467A>G	XP_006720790.1:p.Met3823Val
XM_011522131.1:c.11242A>G	XP_011520433.1:p.Met3748Val
XM_011522132.1:c.9241A>G	XP_011520434.1:p.Met3081Val
XM_011522133.1:c.8470A>G	XP_011520435.1:p.Met2824Val
XM_011522134.1:c.5842A>G	XP_011520436.1:p.Met1948Val
XM_005268276.5:c.11611A>G	XP_005268333.1:p.Met3871Val
XM_006720726.3:c.11710A>G	XP_006720789.1:p.Met3904Val
XM_006720727.3:c.11467A>G	XP_006720790.1:p.Met3823Val
XM_017022695.1:c.11611A>G	XP_016878184.1:p.Met3871Val
XM_017022696.1:c.11611A>G	XP_016878185.1:p.Met3871Val
XM_017022697.1:c.4891A>G	XP_016878186.1:p.Met1631Val
XM_017022698.1:c.4891A>G	XP_016878187.1:p.Met1631Val
NM_004667.6:c.11725A>G MANE Select	NP_004658.3:p.Met3909Val