Canonical Allele Identifier: CA410898798

Gene: IGLL1

Linked Data

• gnomAD v4: 22-23573493-C-A
• MyVariant Identifiers: chr22:g.23915680C>A (hg19) ; chr22:g.23573493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573493C>A , CM000684.2:g.23573493C>A	GRCh38
NC_000022.10:g.23915680C>A , CM000684.1:g.23915680C>A	GRCh37
NC_000022.9:g.22245680C>A	NCBI36
NG_009791.1:g.11816G>T , LRG_69:g.11816G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330377.3:c.415G>T MANE Select	ENSP00000329312.2:p.Asp139Tyr
ENST00000249053.3:c.*44G>T	ENSP00000249053.3:n.*44G>T
ENST00000330377.2:c.415G>T	ENSP00000329312.2:p.Asp139Tyr
ENST00000438703.1:c.418G>T	ENSP00000403391.1:p.Asp140Tyr
NM_020070.3:c.415G>T	NP_064455.1:p.Asp139Tyr
NM_152855.2:c.*44G>T	NP_690594.1:n.*44G>T
XM_011530169.1:c.418G>T	XP_011528471.1:p.Asp140Tyr
XM_011530169.2:c.418G>T	XP_011528471.1:p.Asp140Tyr
NM_020070.4:c.415G>T MANE Select	NP_064455.1:p.Asp139Tyr
NM_001369906.1:c.418G>T	NP_001356835.1:p.Asp140Tyr
NM_152855.3:c.*44G>T	NP_690594.1:n.*44G>T