Canonical Allele Identifier: CA363496087

Gene: NEU1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31862079A>G , CM000668.2:g.31862079A>G	GRCh38
NC_000006.11:g.31829856A>G , CM000668.1:g.31829856A>G	GRCh37
NC_000006.10:g.31937835A>G	NCBI36
NG_008201.1:g.5854T>C
NG_023058.1:g.21968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.272T>C MANE Select	ENSP00000364782.4:p.Leu91Pro
ENST00000677054.1:n.401T>C
ENST00000677512.1:n.380T>C
ENST00000678869.1:n.380T>C
ENST00000375631.4:c.272T>C	ENSP00000364782.4:p.Leu91Pro
ENST00000480384.1:n.301T>C
ENST00000491768.5:c.272T>C	ENSP00000433127.1:p.Leu91Pro
ENST00000495807.1:n.292T>C
NM_000434.3:c.272T>C	NP_000425.1:p.Leu91Pro
NM_000434.4:c.272T>C MANE Select	NP_000425.1:p.Leu91Pro