Canonical Allele Identifier: CA391381957

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386947C>A (hg19) ; chr15:g.28141801C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141801C>A , CM000677.2:g.28141801C>A	GRCh38
NC_000015.9:g.28386947C>A , CM000677.1:g.28386947C>A	GRCh37
NC_000015.8:g.26060542C>A	NCBI36
NG_016355.1:g.185349G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11746G>T MANE Select	ENSP00000261609.8:p.Asp3916Tyr
ENST00000650509.1:c.3457G>T	ENSP00000496936.1:p.Asp1153Tyr
ENST00000261609.11:c.11746G>T	ENSP00000261609.7:p.Asp3916Tyr
ENST00000564519.1:n.261G>T
NM_004667.5:c.11746G>T	NP_004658.3:p.Asp3916Tyr
XM_005268276.3:c.11632G>T	XP_005268333.1:p.Asp3878Tyr
XM_005268277.3:c.11632G>T	XP_005268334.1:p.Asp3878Tyr
XM_006720726.2:c.11731G>T	XP_006720789.1:p.Asp3911Tyr
XM_006720727.2:c.11488G>T	XP_006720790.1:p.Asp3830Tyr
XM_011522131.1:c.11263G>T	XP_011520433.1:p.Asp3755Tyr
XM_011522132.1:c.9262G>T	XP_011520434.1:p.Asp3088Tyr
XM_011522133.1:c.8491G>T	XP_011520435.1:p.Asp2831Tyr
XM_011522134.1:c.5863G>T	XP_011520436.1:p.Asp1955Tyr
XM_005268276.5:c.11632G>T	XP_005268333.1:p.Asp3878Tyr
XM_006720726.3:c.11731G>T	XP_006720789.1:p.Asp3911Tyr
XM_006720727.3:c.11488G>T	XP_006720790.1:p.Asp3830Tyr
XM_017022695.1:c.11632G>T	XP_016878184.1:p.Asp3878Tyr
XM_017022696.1:c.11632G>T	XP_016878185.1:p.Asp3878Tyr
XM_017022697.1:c.4912G>T	XP_016878186.1:p.Asp1638Tyr
XM_017022698.1:c.4912G>T	XP_016878187.1:p.Asp1638Tyr
NM_004667.6:c.11746G>T MANE Select	NP_004658.3:p.Asp3916Tyr