Canonical Allele Identifier: CA352913022
Gene: GNAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1352647422
gnomAD v2: 3-50230741-T-C
gnomAD v4: 3-50193308-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193308T>C , CM000665.2:g.50193308T>C GRCh38
NC_000003.11:g.50230741T>C , CM000665.1:g.50230741T>C GRCh37
NC_000003.10:g.50205745T>C NCBI36
NG_009831.1:g.6699T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.193T>C MANE Select ENSP00000232461.3:p.Phe65Leu
ENST00000232461.7:c.193T>C ENSP00000232461.3:p.Phe65Leu
ENST00000433068.5:c.193T>C ENSP00000387555.1:p.Phe65Leu
ENST00000440836.1:c.49T>C ENSP00000403537.1:p.Phe17Leu
NM_000172.3:c.193T>C NP_000163.2:p.Phe65Leu
NM_144499.2:c.193T>C NP_653082.1:p.Phe65Leu
XM_011533595.1:c.49T>C XP_011531897.1:p.Phe17Leu
XM_011533596.1:c.49T>C XP_011531898.1:p.Phe17Leu
XR_940416.1:n.473T>C
NM_000172.4:c.193T>C NP_000163.2:p.Phe65Leu
NM_144499.3:c.193T>C MANE Select NP_653082.1:p.Phe65Leu