Canonical Allele Identifier: CA2658869005
Gene: SIX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44942031_44942048dup , CM000664.2:g.44942031_44942048dup GRCh38
NC_000002.11:g.45169170_45169187dup , CM000664.1:g.45169170_45169187dup GRCh37
NC_000002.10:g.45022674_45022691dup NCBI36
NG_016222.1:g.5134_5151dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260653.5:c.-74_-57dup MANE Select ENSP00000260653.3:n.-74_-57dup
ENST00000260653.4:c.-74_-57dup ENSP00000260653.3:n.-74_-57dup
NM_005413.3:c.-74_-57dup NP_005404.1:n.-74_-57dup
XM_011533042.1:c.-74_-57dup XP_011531344.1:n.-74_-57dup
NM_005413.4:c.-74_-57dup MANE Select NP_005404.1:n.-74_-57dup