Canonical Allele Identifier: CA352913756
Gene: GNAT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.50230801A>G (hg19) chr3:g.50193368A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50193368A>G , CM000665.2:g.50193368A>G GRCh38
NC_000003.11:g.50230801A>G , CM000665.1:g.50230801A>G GRCh37
NC_000003.10:g.50205805A>G NCBI36
NG_009831.1:g.6759A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000232461.8:c.253A>G MANE Select ENSP00000232461.3:p.Thr85Ala
ENST00000232461.7:c.253A>G ENSP00000232461.3:p.Thr85Ala
ENST00000433068.5:c.253A>G ENSP00000387555.1:p.Thr85Ala
ENST00000440836.1:c.109A>G ENSP00000403537.1:p.Thr37Ala
NM_000172.3:c.253A>G NP_000163.2:p.Thr85Ala
NM_144499.2:c.253A>G NP_653082.1:p.Thr85Ala
XM_011533595.1:c.109A>G XP_011531897.1:p.Thr37Ala
XM_011533596.1:c.109A>G XP_011531898.1:p.Thr37Ala
XR_940416.1:n.533A>G
NM_000172.4:c.253A>G NP_000163.2:p.Thr85Ala
NM_144499.3:c.253A>G MANE Select NP_653082.1:p.Thr85Ala
Search 100 bp 5'
Search 100 bp 3'