Canonical Allele Identifier: CA391381992

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386961T>A (hg19) ; chr15:g.28141815T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141815T>A , CM000677.2:g.28141815T>A	GRCh38
NC_000015.9:g.28386961T>A , CM000677.1:g.28386961T>A	GRCh37
NC_000015.8:g.26060556T>A	NCBI36
NG_016355.1:g.185335A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11732A>T MANE Select	ENSP00000261609.8:p.Asp3911Val
ENST00000650509.1:c.3443A>T	ENSP00000496936.1:p.Asp1148Val
ENST00000261609.11:c.11732A>T	ENSP00000261609.7:p.Asp3911Val
ENST00000564519.1:n.247A>T
NM_004667.5:c.11732A>T	NP_004658.3:p.Asp3911Val
XM_005268276.3:c.11618A>T	XP_005268333.1:p.Asp3873Val
XM_005268277.3:c.11618A>T	XP_005268334.1:p.Asp3873Val
XM_006720726.2:c.11717A>T	XP_006720789.1:p.Asp3906Val
XM_006720727.2:c.11474A>T	XP_006720790.1:p.Asp3825Val
XM_011522131.1:c.11249A>T	XP_011520433.1:p.Asp3750Val
XM_011522132.1:c.9248A>T	XP_011520434.1:p.Asp3083Val
XM_011522133.1:c.8477A>T	XP_011520435.1:p.Asp2826Val
XM_011522134.1:c.5849A>T	XP_011520436.1:p.Asp1950Val
XM_005268276.5:c.11618A>T	XP_005268333.1:p.Asp3873Val
XM_006720726.3:c.11717A>T	XP_006720789.1:p.Asp3906Val
XM_006720727.3:c.11474A>T	XP_006720790.1:p.Asp3825Val
XM_017022695.1:c.11618A>T	XP_016878184.1:p.Asp3873Val
XM_017022696.1:c.11618A>T	XP_016878185.1:p.Asp3873Val
XM_017022697.1:c.4898A>T	XP_016878186.1:p.Asp1633Val
XM_017022698.1:c.4898A>T	XP_016878187.1:p.Asp1633Val
NM_004667.6:c.11732A>T MANE Select	NP_004658.3:p.Asp3911Val