Canonical Allele Identifier: CA2577853738
Gene: GNAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193039A>T , CM000665.2:g.50193039A>T GRCh38
NC_000003.11:g.50230472A>T , CM000665.1:g.50230472A>T GRCh37
NC_000003.10:g.50205476A>T NCBI36
NG_009831.1:g.6430A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000232461.8:c.107-94A>T MANE Select ENSP00000232461.3:n.107-94A>T
ENST00000232461.7:c.107-94A>T ENSP00000232461.3:n.107-94A>T
ENST00000433068.5:c.107-94A>T ENSP00000387555.1:n.107-94A>T
ENST00000440836.1:c.-38-94A>T ENSP00000403537.1:n.-38-94A>T
ENST00000467787.1:n.287+55A>T
NM_000172.3:c.107-94A>T NP_000163.2:n.107-94A>T
NM_144499.2:c.107-94A>T NP_653082.1:n.107-94A>T
XM_011533595.1:c.-39+55A>T XP_011531897.1:n.-39+55A>T
XM_011533596.1:c.-39+55A>T XP_011531898.1:n.-39+55A>T
XR_940416.1:n.386+55A>T
NM_000172.4:c.107-94A>T NP_000163.2:n.107-94A>T
NM_144499.3:c.107-94A>T MANE Select NP_653082.1:n.107-94A>T