Canonical Allele Identifier: CA2166479580

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141118_28141119delinsAT , CM000677.2:g.28141118_28141119delinsAT	GRCh38
NC_000015.9:g.28386264_28386265delinsAT , CM000677.1:g.28386264_28386265delinsAT	GRCh37
NC_000015.8:g.26059859_26059860delinsAT	NCBI36
NG_016355.1:g.186031_186032delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.12015+313_12015+314delinsAT MANE Select	ENSP00000261609.8:n.12015+313_12015+314delinsAT
ENST00000650509.1:c.3726+313_3726+314delinsAT	ENSP00000496936.1:n.3726+313_3726+314delinsAT
ENST00000261609.11:c.12015+313_12015+314delinsAT	ENSP00000261609.7:n.12015+313_12015+314delinsAT
NM_004667.5:c.12015+313_12015+314delinsAT	NP_004658.3:n.12015+313_12015+314delinsAT
XM_005268276.3:c.11901+313_11901+314delinsAT	XP_005268333.1:n.11901+313_11901+314delinsAT
XM_005268277.3:c.11901+313_11901+314delinsAT	XP_005268334.1:n.11901+313_11901+314delinsAT
XM_006720726.2:c.12000+313_12000+314delinsAT	XP_006720789.1:n.12000+313_12000+314delinsAT
XM_006720727.2:c.11757+313_11757+314delinsAT	XP_006720790.1:n.11757+313_11757+314delinsAT
XM_011522131.1:c.11532+313_11532+314delinsAT	XP_011520433.1:n.11532+313_11532+314delinsAT
XM_011522132.1:c.9531+313_9531+314delinsAT	XP_011520434.1:n.9531+313_9531+314delinsAT
XM_011522133.1:c.8760+313_8760+314delinsAT	XP_011520435.1:n.8760+313_8760+314delinsAT
XM_011522134.1:c.6132+313_6132+314delinsAT	XP_011520436.1:n.6132+313_6132+314delinsAT
XM_005268276.5:c.11901+313_11901+314delinsAT	XP_005268333.1:n.11901+313_11901+314delinsAT
XM_006720726.3:c.12000+313_12000+314delinsAT	XP_006720789.1:n.12000+313_12000+314delinsAT
XM_006720727.3:c.11757+313_11757+314delinsAT	XP_006720790.1:n.11757+313_11757+314delinsAT
XM_017022695.1:c.11901+313_11901+314delinsAT	XP_016878184.1:n.11901+313_11901+314delinsAT
XM_017022696.1:c.11901+313_11901+314delinsAT	XP_016878185.1:n.11901+313_11901+314delinsAT
XM_017022697.1:c.5181+313_5181+314delinsAT	XP_016878186.1:n.5181+313_5181+314delinsAT
XM_017022698.1:c.5181+313_5181+314delinsAT	XP_016878187.1:n.5181+313_5181+314delinsAT
NM_004667.6:c.12015+313_12015+314delinsAT MANE Select	NP_004658.3:n.12015+313_12015+314delinsAT