Canonical Allele Identifier: CA96900252
Gene: NMU HGNC NCBI

Linked Data

dbSNP Id: rs13434995
gnomAD v2: 4-56467214-A-G
gnomAD v3: 4-55601047-A-G
gnomAD v4: 4-55601047-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55601047A>G , CM000666.2:g.55601047A>G GRCh38
NC_000004.11:g.56467214A>G , CM000666.1:g.56467214A>G GRCh37
NC_000004.10:g.56161971A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264218.7:c.436-472T>C MANE Select ENSP00000264218.3:n.436-472T>C
ENST00000505262.5:c.355-472T>C ENSP00000424246.1:n.355-472T>C
ENST00000507338.1:c.361-472T>C ENSP00000422870.1:n.361-472T>C
ENST00000509371.1:n.200-472T>C
ENST00000511469.5:c.388-472T>C ENSP00000422399.1:n.388-472T>C
ENST00000515325.5:n.428-472T>C
NM_001292045.1:c.388-472T>C NP_001278974.1:n.388-472T>C
NM_001292046.1:c.361-472T>C NP_001278975.1:n.361-472T>C
NM_006681.3:c.436-472T>C NP_006672.1:n.436-472T>C
NR_120489.1:n.428-472T>C
XM_011534367.1:c.385-472T>C XP_011532669.1:n.385-472T>C
XM_011534368.1:c.334-472T>C XP_011532670.1:n.334-472T>C
XM_011534367.2:c.385-472T>C XP_011532669.1:n.385-472T>C
XM_011534368.3:c.334-472T>C XP_011532670.1:n.334-472T>C
NM_006681.4:c.436-472T>C MANE Select NP_006672.1:n.436-472T>C
NM_001292045.2:c.388-472T>C NP_001278974.1:n.388-472T>C
NM_001292046.2:c.361-472T>C NP_001278975.1:n.361-472T>C
NR_120489.2:n.523-472T>C