Canonical Allele Identifier: CA513685757

Gene: IGLL1

Linked Data

• MyVariant Identifiers: chr22:g.23915477C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573290C>A , CM000684.2:g.23573290C>A	GRCh38
NC_000022.10:g.23915477C>A , CM000684.1:g.23915477C>A	GRCh37
NC_000022.9:g.22245477C>A	NCBI36
NG_009791.1:g.12019G>T , LRG_69:g.12019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330377.3:c.618G>T MANE Select	ENSP00000329312.2:p.Thr206=
ENST00000249053.3:c.*247G>T	ENSP00000249053.3:n.*247G>T
ENST00000330377.2:c.618G>T	ENSP00000329312.2:p.Thr206=
NM_020070.3:c.618G>T	NP_064455.1:p.Thr206=
NM_152855.2:c.*247G>T	NP_690594.1:n.*247G>T
XM_011530169.1:c.621G>T	XP_011528471.1:p.Thr207=
XM_011530169.2:c.621G>T	XP_011528471.1:p.Thr207=
NM_020070.4:c.618G>T MANE Select	NP_064455.1:p.Thr206=
NM_001369906.1:c.621G>T	NP_001356835.1:p.Thr207=
NM_152855.3:c.*247G>T	NP_690594.1:n.*247G>T