Canonical Allele Identifier: CA2678053939

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861554-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861554C>G , CM000668.2:g.31861554C>G	GRCh38
NC_000006.11:g.31829331C>G , CM000668.1:g.31829331C>G	GRCh37
NC_000006.10:g.31937310C>G	NCBI36
NG_008201.1:g.6379G>C
NG_023058.1:g.22493G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-104G>C MANE Select	ENSP00000364782.4:n.353-104G>C
ENST00000677054.1:n.926G>C
ENST00000677512.1:n.461-104G>C
ENST00000678869.1:n.461-104G>C
ENST00000375631.4:c.353-104G>C	ENSP00000364782.4:n.353-104G>C
ENST00000480384.1:n.382-104G>C
ENST00000491768.5:c.353-104G>C	ENSP00000433127.1:n.353-104G>C
ENST00000495807.1:n.817G>C
NM_000434.3:c.353-104G>C	NP_000425.1:n.353-104G>C
NM_000434.4:c.353-104G>C MANE Select	NP_000425.1:n.353-104G>C