Canonical Allele Identifier: CA363494769

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31829146T>G (hg19) ; chr6:g.31861369T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861369T>G , CM000668.2:g.31861369T>G	GRCh38
NC_000006.11:g.31829146T>G , CM000668.1:g.31829146T>G	GRCh37
NC_000006.10:g.31937125T>G	NCBI36
NG_008201.1:g.6564A>C
NG_023058.1:g.22678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.434A>C MANE Select	ENSP00000364782.4:p.Asp145Ala
ENST00000677054.1:n.1111A>C
ENST00000677512.1:n.542A>C
ENST00000678869.1:n.542A>C
ENST00000375631.4:c.434A>C	ENSP00000364782.4:p.Asp145Ala
ENST00000480384.1:n.463A>C
ENST00000491768.5:c.434A>C	ENSP00000433127.1:p.Asp145Ala
ENST00000495807.1:n.1002A>C
NM_000434.3:c.434A>C	NP_000425.1:p.Asp145Ala
NM_000434.4:c.434A>C MANE Select	NP_000425.1:p.Asp145Ala