Canonical Allele Identifier: CA413664726
Gene: NEXMIF HGNC NCBI

Linked Data

gnomAD v4: X-74740758-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740758G>C , CM000685.2:g.74740758G>C GRCh38
NC_000023.10:g.73960593G>C , CM000685.1:g.73960593G>C GRCh37
NC_000023.9:g.73877318G>C NCBI36
NG_027726.1:g.189695C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3799C>G MANE Select ENSP00000055682.5:p.Pro1267Ala
ENST00000616200.2:c.3799C>G ENSP00000480284.1:p.Pro1267Ala
ENST00000642681.2:c.3799C>G ENSP00000495800.1:p.Pro1267Ala
ENST00000055682.10:c.3799C>G ENSP00000055682.5:p.Pro1267Ala
ENST00000616200.1:c.3799C>G ENSP00000480284.1:p.Pro1267Ala
NM_001008537.2:c.3799C>G NP_001008537.1:p.Pro1267Ala
XM_011530935.1:c.3799C>G XP_011529237.1:p.Pro1267Ala
NM_001008537.3:c.3799C>G MANE Select NP_001008537.1:p.Pro1267Ala