Canonical Allele Identifier: CA363491730

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31828249C>G (hg19) ; chr6:g.31860472C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860472C>G , CM000668.2:g.31860472C>G	GRCh38
NC_000006.11:g.31828249C>G , CM000668.1:g.31828249C>G	GRCh37
NC_000006.10:g.31936228C>G	NCBI36
NG_008201.1:g.7461G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.765G>C MANE Select	ENSP00000364782.4:p.Lys255Asn
ENST00000677054.1:n.2008G>C
ENST00000677512.1:n.873G>C
ENST00000678869.1:n.1439G>C
ENST00000375631.4:c.765G>C	ENSP00000364782.4:p.Lys255Asn
ENST00000480384.1:n.794G>C
ENST00000491768.5:c.765G>C	ENSP00000433127.1:p.Lys255Asn
ENST00000495807.1:n.1899G>C
NM_000434.3:c.765G>C	NP_000425.1:p.Lys255Asn
NM_000434.4:c.765G>C MANE Select	NP_000425.1:p.Lys255Asn