Canonical Allele Identifier: CA1162766

Gene: NAXE

Linked Data

• dbSNP Id: rs780668270
• ExAC: 1:156562344 C / T
• gnomAD v2: 1-156562344-C-T
• gnomAD v4: 1-156592552-C-T
• MyVariant Identifiers: chr1:g.156562344C>T (hg19) ; chr1:g.156592552C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156592552C>T , CM000663.2:g.156592552C>T	GRCh38
NC_000001.10:g.156562344C>T , CM000663.1:g.156562344C>T	GRCh37
NC_000001.9:g.154828968C>T	NCBI36
NG_052542.1:g.5787C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368235.8:c.403-5C>T MANE Select	ENSP00000357218.3:n.403-5C>T
ENST00000467374.2:n.508C>T
ENST00000679369.1:c.292-5C>T	ENSP00000505883.1:n.292-5C>T
ENST00000679649.1:n.442-5C>T
ENST00000679702.1:c.403-5C>T	ENSP00000505913.1:n.403-5C>T
ENST00000679913.1:n.607-5C>T
ENST00000680004.1:c.403-5C>T	ENSP00000506275.1:n.403-5C>T
ENST00000680087.1:c.403-5C>T	ENSP00000505907.1:n.403-5C>T
ENST00000680269.1:c.403-5C>T	ENSP00000505899.1:n.403-5C>T
ENST00000680529.1:n.587-5C>T
ENST00000680661.1:c.403-5C>T	ENSP00000505088.1:n.403-5C>T
ENST00000681054.1:c.403-5C>T	ENSP00000506192.1:n.403-5C>T
ENST00000681523.1:c.403-5C>T	ENSP00000505349.1:n.403-5C>T
ENST00000681645.1:n.442-5C>T
ENST00000681734.1:c.403-5C>T	ENSP00000506177.1:n.403-5C>T
ENST00000681825.1:n.207-5C>T
ENST00000681922.1:n.442-5C>T
ENST00000368233.3:c.403-5C>T	ENSP00000357216.3:n.403-5C>T
ENST00000368234.7:c.403-5C>T	ENSP00000357217.3:n.403-5C>T
ENST00000368235.7:c.403-5C>T	ENSP00000357218.3:n.403-5C>T
ENST00000467374.1:n.312-5C>T
NM_144772.2:c.403-5C>T	NP_658985.2:n.403-5C>T
XM_017000319.2:c.403-5C>T	XP_016855808.1:n.403-5C>T
NM_144772.3:c.403-5C>T MANE Select	NP_658985.2:n.403-5C>T