Canonical Allele Identifier: CA2166480054

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141718_28141723delinsCTAATA , CM000677.2:g.28141718_28141723delinsCTAATA	GRCh38
NC_000015.9:g.28386864_28386869delinsCTAATA , CM000677.1:g.28386864_28386869delinsCTAATA	GRCh37
NC_000015.8:g.26060459_26060464delinsCTAATA	NCBI36
NG_016355.1:g.185427_185432delinsTATTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11816+8_11816+13delinsTATTAG MANE Select	ENSP00000261609.8:n.11816+8_11816+13delinsTATTAG
ENST00000650509.1:c.3527+8_3527+13delinsTATTAG	ENSP00000496936.1:n.3527+8_3527+13delinsTATTAG
ENST00000261609.11:c.11816+8_11816+13delinsTATTAG	ENSP00000261609.7:n.11816+8_11816+13delinsTATTAG
NM_004667.5:c.11816+8_11816+13delinsTATTAG	NP_004658.3:n.11816+8_11816+13delinsTATTAG
XM_005268276.3:c.11702+8_11702+13delinsTATTAG	XP_005268333.1:n.11702+8_11702+13delinsTATTAG
XM_005268277.3:c.11702+8_11702+13delinsTATTAG	XP_005268334.1:n.11702+8_11702+13delinsTATTAG
XM_006720726.2:c.11801+8_11801+13delinsTATTAG	XP_006720789.1:n.11801+8_11801+13delinsTATTAG
XM_006720727.2:c.11558+8_11558+13delinsTATTAG	XP_006720790.1:n.11558+8_11558+13delinsTATTAG
XM_011522131.1:c.11333+8_11333+13delinsTATTAG	XP_011520433.1:n.11333+8_11333+13delinsTATTAG
XM_011522132.1:c.9332+8_9332+13delinsTATTAG	XP_011520434.1:n.9332+8_9332+13delinsTATTAG
XM_011522133.1:c.8561+8_8561+13delinsTATTAG	XP_011520435.1:n.8561+8_8561+13delinsTATTAG
XM_011522134.1:c.5933+8_5933+13delinsTATTAG	XP_011520436.1:n.5933+8_5933+13delinsTATTAG
XM_005268276.5:c.11702+8_11702+13delinsTATTAG	XP_005268333.1:n.11702+8_11702+13delinsTATTAG
XM_006720726.3:c.11801+8_11801+13delinsTATTAG	XP_006720789.1:n.11801+8_11801+13delinsTATTAG
XM_006720727.3:c.11558+8_11558+13delinsTATTAG	XP_006720790.1:n.11558+8_11558+13delinsTATTAG
XM_017022695.1:c.11702+8_11702+13delinsTATTAG	XP_016878184.1:n.11702+8_11702+13delinsTATTAG
XM_017022696.1:c.11702+8_11702+13delinsTATTAG	XP_016878185.1:n.11702+8_11702+13delinsTATTAG
XM_017022697.1:c.4982+8_4982+13delinsTATTAG	XP_016878186.1:n.4982+8_4982+13delinsTATTAG
XM_017022698.1:c.4982+8_4982+13delinsTATTAG	XP_016878187.1:n.4982+8_4982+13delinsTATTAG
NM_004667.6:c.11816+8_11816+13delinsTATTAG MANE Select	NP_004658.3:n.11816+8_11816+13delinsTATTAG