Canonical Allele Identifier: CA96900355

Gene: NMU

Linked Data

• dbSNP Id: rs539035440
• gnomAD v2: 4-56467404-T-C
• gnomAD v3: 4-55601237-T-C
• gnomAD v4: 4-55601237-T-C
• MyVariant Identifiers: chr4:g.56467404T>C (hg19) ; chr4:g.55601237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55601237T>C , CM000666.2:g.55601237T>C	GRCh38
NC_000004.11:g.56467404T>C , CM000666.1:g.56467404T>C	GRCh37
NC_000004.10:g.56162161T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264218.7:c.436-662A>G MANE Select	ENSP00000264218.3:n.436-662A>G
ENST00000505262.5:c.355-662A>G	ENSP00000424246.1:n.355-662A>G
ENST00000507338.1:c.361-662A>G	ENSP00000422870.1:n.361-662A>G
ENST00000509371.1:n.200-662A>G
ENST00000511469.5:c.388-662A>G	ENSP00000422399.1:n.388-662A>G
ENST00000515325.5:n.428-662A>G
NM_001292045.1:c.388-662A>G	NP_001278974.1:n.388-662A>G
NM_001292046.1:c.361-662A>G	NP_001278975.1:n.361-662A>G
NM_006681.3:c.436-662A>G	NP_006672.1:n.436-662A>G
NR_120489.1:n.428-662A>G
XM_011534367.1:c.385-662A>G	XP_011532669.1:n.385-662A>G
XM_011534368.1:c.334-662A>G	XP_011532670.1:n.334-662A>G
XM_011534367.2:c.385-662A>G	XP_011532669.1:n.385-662A>G
XM_011534368.3:c.334-662A>G	XP_011532670.1:n.334-662A>G
NM_006681.4:c.436-662A>G MANE Select	NP_006672.1:n.436-662A>G
NM_001292045.2:c.388-662A>G	NP_001278974.1:n.388-662A>G
NM_001292046.2:c.361-662A>G	NP_001278975.1:n.361-662A>G
NR_120489.2:n.523-662A>G