Canonical Allele Identifier: CA1363836795
Gene: GNAT1 HGNC NCBI

Linked Data

dbSNP Id: rs797005370

Genomic Alleles

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

Transcript Alleles

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