Canonical Allele Identifier: CA2649046614
Gene: SELE HGNC NCBI
FIRRM HGNC NCBI

Linked Data

gnomAD v4: 1-169731744-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169731744G>A , CM000663.2:g.169731744G>A GRCh38
NC_000001.10:g.169700885G>A , CM000663.1:g.169700885G>A GRCh37
NC_000001.9:g.167967509G>A NCBI36
NG_012124.1:g.7336C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000333360.12:c.529+91C>T (SELE) MANE Select ENSP00000331736.7:n.529+91C>T
ENST00000333360.11:c.529+91C>T (SELE) ENSP00000331736.7:n.529+91C>T
ENST00000367774.1:c.529+91C>T (SELE) ENSP00000356748.1:n.529+91C>T
ENST00000367775.5:c.529+91C>T (SELE) ENSP00000356749.1:n.529+91C>T
ENST00000367776.5:c.529+91C>T (SELE) ENSP00000356750.1:n.529+91C>T
ENST00000367777.5:c.529+91C>T (SELE) ENSP00000356751.1:n.529+91C>T
ENST00000461085.1:n.303C>T (SELE)
ENST00000498289.5:n.851+47812G>A (FIRRM)
NM_000450.2:c.529+91C>T (SELE) MANE Select NP_000441.2:n.529+91C>T
Search 100 bp 5'
Search 100 bp 3'