Canonical Allele Identifier: CA391381446

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386706C>T (hg19) ; chr15:g.28141560C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141560C>T , CM000677.2:g.28141560C>T	GRCh38
NC_000015.9:g.28386706C>T , CM000677.1:g.28386706C>T	GRCh37
NC_000015.8:g.26060301C>T	NCBI36
NG_016355.1:g.185590G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11887G>A MANE Select	ENSP00000261609.8:p.Gly3963Ser
ENST00000650509.1:c.3598G>A	ENSP00000496936.1:p.Gly1200Ser
ENST00000261609.11:c.11887G>A	ENSP00000261609.7:p.Gly3963Ser
NM_004667.5:c.11887G>A	NP_004658.3:p.Gly3963Ser
XM_005268276.3:c.11773G>A	XP_005268333.1:p.Gly3925Ser
XM_005268277.3:c.11773G>A	XP_005268334.1:p.Gly3925Ser
XM_006720726.2:c.11872G>A	XP_006720789.1:p.Gly3958Ser
XM_006720727.2:c.11629G>A	XP_006720790.1:p.Gly3877Ser
XM_011522131.1:c.11404G>A	XP_011520433.1:p.Gly3802Ser
XM_011522132.1:c.9403G>A	XP_011520434.1:p.Gly3135Ser
XM_011522133.1:c.8632G>A	XP_011520435.1:p.Gly2878Ser
XM_011522134.1:c.6004G>A	XP_011520436.1:p.Gly2002Ser
XM_005268276.5:c.11773G>A	XP_005268333.1:p.Gly3925Ser
XM_006720726.3:c.11872G>A	XP_006720789.1:p.Gly3958Ser
XM_006720727.3:c.11629G>A	XP_006720790.1:p.Gly3877Ser
XM_017022695.1:c.11773G>A	XP_016878184.1:p.Gly3925Ser
XM_017022696.1:c.11773G>A	XP_016878185.1:p.Gly3925Ser
XM_017022697.1:c.5053G>A	XP_016878186.1:p.Gly1685Ser
XM_017022698.1:c.5053G>A	XP_016878187.1:p.Gly1685Ser
NM_004667.6:c.11887G>A MANE Select	NP_004658.3:p.Gly3963Ser