Canonical Allele Identifier: CA449808307

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31828291G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860514G>C , CM000668.2:g.31860514G>C	GRCh38
NC_000006.11:g.31828291G>C , CM000668.1:g.31828291G>C	GRCh37
NC_000006.10:g.31936270G>C	NCBI36
NG_008201.1:g.7419C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.723C>G MANE Select	ENSP00000364782.4:p.Arg241=
ENST00000677054.1:n.1966C>G
ENST00000677512.1:n.831C>G
ENST00000678869.1:n.1397C>G
ENST00000375631.4:c.723C>G	ENSP00000364782.4:p.Arg241=
ENST00000480384.1:n.752C>G
ENST00000491768.5:c.723C>G	ENSP00000433127.1:p.Arg241=
ENST00000495807.1:n.1857C>G
NM_000434.3:c.723C>G	NP_000425.1:p.Arg241=
NM_000434.4:c.723C>G MANE Select	NP_000425.1:p.Arg241=