Canonical Allele Identifier: CA2665814575
Gene: GNAT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193051del , CM000665.2:g.50193051del GRCh38
NC_000003.11:g.50230484del , CM000665.1:g.50230484del GRCh37
NC_000003.10:g.50205488del NCBI36
NG_009831.1:g.6442del

Transcript Alleles

HGVS Amino-acid change
ENST00000232461.8:c.107-82del MANE Select ENSP00000232461.3:n.107-82del
ENST00000232461.7:c.107-82del ENSP00000232461.3:n.107-82del
ENST00000433068.5:c.107-82del ENSP00000387555.1:n.107-82del
ENST00000440836.1:c.-38-82del ENSP00000403537.1:n.-38-82del
ENST00000467787.1:n.287+67del
NM_000172.3:c.107-82del NP_000163.2:n.107-82del
NM_144499.2:c.107-82del NP_653082.1:n.107-82del
XM_011533595.1:c.-39+67del XP_011531897.1:n.-39+67del
XM_011533596.1:c.-39+67del XP_011531898.1:n.-39+67del
XR_940416.1:n.386+67del
NM_000172.4:c.107-82del NP_000163.2:n.107-82del
NM_144499.3:c.107-82del MANE Select NP_653082.1:n.107-82del