Canonical Allele Identifier: CA2756206784
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193428dup , CM000665.2:g.50193428dup GRCh38
NC_000003.11:g.50230861dup , CM000665.1:g.50230861dup GRCh37
NC_000003.10:g.50205865dup NCBI36
NG_009831.1:g.6819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.291+22dup MANE Select ENSP00000232461.3:n.291+22dup
ENST00000232461.7:c.291+22dup ENSP00000232461.3:n.291+22dup
ENST00000433068.5:c.291+22dup ENSP00000387555.1:n.291+22dup
ENST00000440836.1:c.147+22dup ENSP00000403537.1:n.147+22dup
NM_000172.3:c.291+22dup NP_000163.2:n.291+22dup
NM_144499.2:c.291+22dup NP_653082.1:n.291+22dup
XM_011533595.1:c.147+22dup XP_011531897.1:n.147+22dup
XM_011533596.1:c.147+22dup XP_011531898.1:n.147+22dup
XR_940416.1:n.571+22dup
NM_000172.4:c.291+22dup NP_000163.2:n.291+22dup
NM_144499.3:c.291+22dup MANE Select NP_653082.1:n.291+22dup