Canonical Allele Identifier: CA15743393

Gene: NUP37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102119753G>C , CM000674.2:g.102119753G>C	GRCh38
NC_000012.11:g.102513531G>C , CM000674.1:g.102513531G>C	GRCh37
NC_000012.10:g.101037661G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000552283.6:c.-66+297C>G MANE Select	ENSP00000448054.1:n.-66+297C>G
ENST00000543021.5:n.40+297C>G
ENST00000548994.1:n.41+297C>G
ENST00000551200.5:n.42+297C>G
ENST00000551744.2:c.-66+297C>G	ENSP00000448086.1:n.-66+297C>G
ENST00000552283.5:c.-66+297C>G	ENSP00000448054.1:n.-66+297C>G
XM_005269144.2:c.-66+297C>G	XP_005269201.1:n.-66+297C>G
XR_944712.1:n.90+297C>G
NM_024057.3:c.-66+297C>G	NP_076962.2:n.-66+297C>G
XR_944712.2:n.82+297C>G
NM_024057.4:c.-66+297C>G MANE Select	NP_076962.2:n.-66+297C>G