Canonical Allele Identifier: CA2389526091
Gene: IGSF5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.39777429C= , CM000683.2:g.39777429C= GRCh38
NC_000021.8:g.41149356C= , CM000683.1:g.41149356C= GRCh37
NC_000021.7:g.40071226C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380588.5:c.719-1661C= MANE Select ENSP00000369962.4:n.719-1661C=
ENST00000380588.4:c.719-1661C= ENSP00000369962.4:n.719-1661C=
ENST00000479378.1:n.825-1661C=
NM_001080444.1:c.719-1661C= NP_001073913.1:n.719-1661C=
XM_011529472.1:c.989-1661C= XP_011527774.1:n.989-1661C=
XM_011529473.1:c.989-1661C= XP_011527775.1:n.989-1661C=
XM_011529472.2:c.989-1661C= XP_011527774.1:n.989-1661C=
NM_001080444.2:c.719-1661C= MANE Select NP_001073913.1:n.719-1661C=
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