Canonical Allele Identifier: CA513685759
Gene: IGLL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.23915480C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573293C>T , CM000684.2:g.23573293C>T GRCh38
NC_000022.10:g.23915480C>T , CM000684.1:g.23915480C>T GRCh37
NC_000022.9:g.22245480C>T NCBI36
NG_009791.1:g.12016G>A , LRG_69:g.12016G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330377.3:c.615G>A MANE Select ENSP00000329312.2:p.Lys205=
ENST00000249053.3:c.*244G>A ENSP00000249053.3:n.*244G>A
ENST00000330377.2:c.615G>A ENSP00000329312.2:p.Lys205=
NM_020070.3:c.615G>A NP_064455.1:p.Lys205=
NM_152855.2:c.*244G>A NP_690594.1:n.*244G>A
XM_011530169.1:c.618G>A XP_011528471.1:p.Lys206=
XM_011530169.2:c.618G>A XP_011528471.1:p.Lys206=
NM_020070.4:c.615G>A MANE Select NP_064455.1:p.Lys205=
NM_001369906.1:c.618G>A NP_001356835.1:p.Lys206=
NM_152855.3:c.*244G>A NP_690594.1:n.*244G>A