Canonical Allele Identifier: CA363494154

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31829047C>A (hg19) ; chr6:g.31861270C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861270C>A , CM000668.2:g.31861270C>A	GRCh38
NC_000006.11:g.31829047C>A , CM000668.1:g.31829047C>A	GRCh37
NC_000006.10:g.31937026C>A	NCBI36
NG_008201.1:g.6663G>T
NG_023058.1:g.22777G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.533G>T MANE Select	ENSP00000364782.4:p.Gly178Val
ENST00000677054.1:n.1210G>T
ENST00000677512.1:n.641G>T
ENST00000678869.1:n.641G>T
ENST00000375631.4:c.533G>T	ENSP00000364782.4:p.Gly178Val
ENST00000480384.1:n.562G>T
ENST00000491768.5:c.533G>T	ENSP00000433127.1:p.Gly178Val
ENST00000495807.1:n.1101G>T
NM_000434.3:c.533G>T	NP_000425.1:p.Gly178Val
NM_000434.4:c.533G>T MANE Select	NP_000425.1:p.Gly178Val