Canonical Allele Identifier: CA391381094

Gene: HERC2

Linked Data

• MyVariant Identifiers: chr15:g.28386628G>A (hg19) ; chr15:g.28141482G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141482G>A , CM000677.2:g.28141482G>A	GRCh38
NC_000015.9:g.28386628G>A , CM000677.1:g.28386628G>A	GRCh37
NC_000015.8:g.26060223G>A	NCBI36
NG_016355.1:g.185668C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.11965C>T MANE Select	ENSP00000261609.8:p.Gln3989Ter
ENST00000650509.1:c.3676C>T	ENSP00000496936.1:p.Gln1226Ter
ENST00000261609.11:c.11965C>T	ENSP00000261609.7:p.Gln3989Ter
NM_004667.5:c.11965C>T	NP_004658.3:p.Gln3989Ter
XM_005268276.3:c.11851C>T	XP_005268333.1:p.Gln3951Ter
XM_005268277.3:c.11851C>T	XP_005268334.1:p.Gln3951Ter
XM_006720726.2:c.11950C>T	XP_006720789.1:p.Gln3984Ter
XM_006720727.2:c.11707C>T	XP_006720790.1:p.Gln3903Ter
XM_011522131.1:c.11482C>T	XP_011520433.1:p.Gln3828Ter
XM_011522132.1:c.9481C>T	XP_011520434.1:p.Gln3161Ter
XM_011522133.1:c.8710C>T	XP_011520435.1:p.Gln2904Ter
XM_011522134.1:c.6082C>T	XP_011520436.1:p.Gln2028Ter
XM_005268276.5:c.11851C>T	XP_005268333.1:p.Gln3951Ter
XM_006720726.3:c.11950C>T	XP_006720789.1:p.Gln3984Ter
XM_006720727.3:c.11707C>T	XP_006720790.1:p.Gln3903Ter
XM_017022695.1:c.11851C>T	XP_016878184.1:p.Gln3951Ter
XM_017022696.1:c.11851C>T	XP_016878185.1:p.Gln3951Ter
XM_017022697.1:c.5131C>T	XP_016878186.1:p.Gln1711Ter
XM_017022698.1:c.5131C>T	XP_016878187.1:p.Gln1711Ter
NM_004667.6:c.11965C>T MANE Select	NP_004658.3:p.Gln3989Ter