Canonical Allele Identifier: CA1619342372

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861578_31861582delinsCACTT , CM000668.2:g.31861578_31861582delinsCACTT	GRCh38
NC_000006.11:g.31829355_31829359delinsCACTT , CM000668.1:g.31829355_31829359delinsCACTT	GRCh37
NC_000006.10:g.31937334_31937338delinsCACTT	NCBI36
NG_008201.1:g.6351_6355delinsAAGTG
NG_023058.1:g.22465_22469delinsAAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-132_353-128delinsAAGTG MANE Select	ENSP00000364782.4:n.353-132_353-128delinsAAGTG
ENST00000677054.1:n.898_902delinsAAGTG
ENST00000677512.1:n.461-132_461-128delinsAAGTG
ENST00000678869.1:n.461-132_461-128delinsAAGTG
ENST00000375631.4:c.353-132_353-128delinsAAGTG	ENSP00000364782.4:n.353-132_353-128delinsAAGTG
ENST00000480384.1:n.382-132_382-128delinsAAGTG
ENST00000491768.5:c.353-132_353-128delinsAAGTG	ENSP00000433127.1:n.353-132_353-128delinsAAGTG
ENST00000495807.1:n.789_793delinsAAGTG
NM_000434.3:c.353-132_353-128delinsAAGTG	NP_000425.1:n.353-132_353-128delinsAAGTG
NM_000434.4:c.353-132_353-128delinsAAGTG MANE Select	NP_000425.1:n.353-132_353-128delinsAAGTG