Canonical Allele Identifier: CA513347923
Community Standard Title: NM_020070.4(IGLL1):c.252C>T (p.Pro84=)
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23575037G>A , CM000684.2:g.23575037G>A GRCh38
NC_000022.10:g.23917224G>A , CM000684.1:g.23917224G>A GRCh37
NC_000022.9:g.22247224G>A NCBI36
NG_009791.1:g.10272C>T , LRG_69:g.10272C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020070.4:c.252C>T MANE Select NP_064455.1:p.Pro84=
ENST00000330377.3:c.252C>T MANE Select ENSP00000329312.2:p.Pro84=
NM_001369906.1:c.255C>T NP_001356835.1:p.Pro85=
NM_020070.3:c.252C>T NP_064455.1:p.Pro84=
NM_152855.2:c.207-1452C>T NP_690594.1:n.207-1452C>T
NM_152855.3:c.207-1452C>T NP_690594.1:n.207-1452C>T
ENST00000249053.3:c.207-1452C>T ENSP00000249053.3:n.207-1452C>T
ENST00000330377.2:c.252C>T ENSP00000329312.2:p.Pro84=
ENST00000438703.1:c.255C>T ENSP00000403391.1:p.Pro85=
XM_011530169.1:c.255C>T XP_011528471.1:p.Pro85=
XM_011530169.2:c.255C>T XP_011528471.1:p.Pro85=