Canonical Allele Identifier: CA391382055

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386989C>T (hg19) ; chr15:g.28141843C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141843C>T , CM000677.2:g.28141843C>T	GRCh38
NC_000015.9:g.28386989C>T , CM000677.1:g.28386989C>T	GRCh37
NC_000015.8:g.26060584C>T	NCBI36
NG_016355.1:g.185307G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11704G>A MANE Select	ENSP00000261609.8:p.Ala3902Thr
ENST00000650509.1:c.3415G>A	ENSP00000496936.1:p.Ala1139Thr
ENST00000261609.11:c.11704G>A	ENSP00000261609.7:p.Ala3902Thr
ENST00000564519.1:n.219G>A
NM_004667.5:c.11704G>A	NP_004658.3:p.Ala3902Thr
XM_005268276.3:c.11590G>A	XP_005268333.1:p.Ala3864Thr
XM_005268277.3:c.11590G>A	XP_005268334.1:p.Ala3864Thr
XM_006720726.2:c.11689G>A	XP_006720789.1:p.Ala3897Thr
XM_006720727.2:c.11446G>A	XP_006720790.1:p.Ala3816Thr
XM_011522131.1:c.11221G>A	XP_011520433.1:p.Ala3741Thr
XM_011522132.1:c.9220G>A	XP_011520434.1:p.Ala3074Thr
XM_011522133.1:c.8449G>A	XP_011520435.1:p.Ala2817Thr
XM_011522134.1:c.5821G>A	XP_011520436.1:p.Ala1941Thr
XM_005268276.5:c.11590G>A	XP_005268333.1:p.Ala3864Thr
XM_006720726.3:c.11689G>A	XP_006720789.1:p.Ala3897Thr
XM_006720727.3:c.11446G>A	XP_006720790.1:p.Ala3816Thr
XM_017022695.1:c.11590G>A	XP_016878184.1:p.Ala3864Thr
XM_017022696.1:c.11590G>A	XP_016878185.1:p.Ala3864Thr
XM_017022697.1:c.4870G>A	XP_016878186.1:p.Ala1624Thr
XM_017022698.1:c.4870G>A	XP_016878187.1:p.Ala1624Thr
NM_004667.6:c.11704G>A MANE Select	NP_004658.3:p.Ala3902Thr