Canonical Allele Identifier: CA2166480065

Gene: HERC2

Linked Data

• dbSNP Id: rs1891246938

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141726_28141729dup , CM000677.2:g.28141726_28141729dup	GRCh38
NC_000015.9:g.28386872_28386875dup , CM000677.1:g.28386872_28386875dup	GRCh37
NC_000015.8:g.26060467_26060470dup	NCBI36
NG_016355.1:g.185422_185425dup

Transcript Alleles

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