Canonical Allele Identifier: CA542849043

Gene: GNAT1

Linked Data

• dbSNP Id: rs1370068957
• gnomAD v2: 3-50230636-C-T
• gnomAD v4: 3-50193203-C-T
• MyVariant Identifiers: chr3:g.50230636C>T (hg19) ; chr3:g.50193203C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50193203C>T , CM000665.2:g.50193203C>T	GRCh38
NC_000003.11:g.50230636C>T , CM000665.1:g.50230636C>T	GRCh37
NC_000003.10:g.50205640C>T	NCBI36
NG_009831.1:g.6594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232461.8:c.149+28C>T MANE Select	ENSP00000232461.3:n.149+28C>T
ENST00000232461.7:c.149+28C>T	ENSP00000232461.3:n.149+28C>T
ENST00000433068.5:c.149+28C>T	ENSP00000387555.1:n.149+28C>T
ENST00000440836.1:c.5+28C>T	ENSP00000403537.1:n.5+28C>T
NM_000172.3:c.149+28C>T	NP_000163.2:n.149+28C>T
NM_144499.2:c.149+28C>T	NP_653082.1:n.149+28C>T
XM_011533595.1:c.5+28C>T	XP_011531897.1:n.5+28C>T
XM_011533596.1:c.5+28C>T	XP_011531898.1:n.5+28C>T
XR_940416.1:n.429+28C>T
NM_000172.4:c.149+28C>T	NP_000163.2:n.149+28C>T
NM_144499.3:c.149+28C>T MANE Select	NP_653082.1:n.149+28C>T