Canonical Allele Identifier: CA517466430
Gene: NEXMIF HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.73960684T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74740849T>C , CM000685.2:g.74740849T>C GRCh38
NC_000023.10:g.73960684T>C , CM000685.1:g.73960684T>C GRCh37
NC_000023.9:g.73877409T>C NCBI36
NG_027726.1:g.189604A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000055682.12:c.3708A>G MANE Select ENSP00000055682.5:p.Lys1236=
ENST00000616200.2:c.3708A>G ENSP00000480284.1:p.Lys1236=
ENST00000642681.2:c.3708A>G ENSP00000495800.1:p.Lys1236=
ENST00000055682.10:c.3708A>G ENSP00000055682.5:p.Lys1236=
ENST00000616200.1:c.3708A>G ENSP00000480284.1:p.Lys1236=
NM_001008537.2:c.3708A>G NP_001008537.1:p.Lys1236=
XM_011530935.1:c.3708A>G XP_011529237.1:p.Lys1236=
NM_001008537.3:c.3708A>G MANE Select NP_001008537.1:p.Lys1236=