Canonical Allele Identifier: CA2665814925
Gene: GNAT1 HGNC NCBI

Linked Data

gnomAD v4: 3-50193189-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193189C>T , CM000665.2:g.50193189C>T GRCh38
NC_000003.11:g.50230622C>T , CM000665.1:g.50230622C>T GRCh37
NC_000003.10:g.50205626C>T NCBI36
NG_009831.1:g.6580C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.149+14C>T MANE Select ENSP00000232461.3:n.149+14C>T
ENST00000232461.7:c.149+14C>T ENSP00000232461.3:n.149+14C>T
ENST00000433068.5:c.149+14C>T ENSP00000387555.1:n.149+14C>T
ENST00000440836.1:c.5+14C>T ENSP00000403537.1:n.5+14C>T
NM_000172.3:c.149+14C>T NP_000163.2:n.149+14C>T
NM_144499.2:c.149+14C>T NP_653082.1:n.149+14C>T
XM_011533595.1:c.5+14C>T XP_011531897.1:n.5+14C>T
XM_011533596.1:c.5+14C>T XP_011531898.1:n.5+14C>T
XR_940416.1:n.429+14C>T
NM_000172.4:c.149+14C>T NP_000163.2:n.149+14C>T
NM_144499.3:c.149+14C>T MANE Select NP_653082.1:n.149+14C>T