Canonical Allele Identifier: CA366022767

Gene: LATS1

Linked Data

• MyVariant Identifiers: chr6:g.150001208A>C (hg19) ; chr6:g.149680072A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149680072A>C , CM000668.2:g.149680072A>C	GRCh38
NC_000006.11:g.150001208A>C , CM000668.1:g.150001208A>C	GRCh37
NC_000006.10:g.150042901A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543571.6:c.2396T>G MANE Select	ENSP00000437550.1:p.Ile799Ser
ENST00000253339.9:c.2396T>G	ENSP00000253339.5:p.Ile799Ser
ENST00000441107.5:c.*2083T>G	ENSP00000403815.1:n.*2083T>G
ENST00000542747.5:n.2233T>G
ENST00000543571.5:c.2396T>G	ENSP00000437550.1:p.Ile799Ser
NM_004690.3:c.2396T>G	NP_004681.1:p.Ile799Ser
NR_073033.1:n.2850T>G
XM_006715603.2:c.2396T>G	XP_006715666.1:p.Ile799Ser
XM_011536250.1:c.2396T>G	XP_011534552.1:p.Ile799Ser
XM_011536251.1:c.2081T>G	XP_011534553.1:p.Ile694Ser
XM_011536252.1:c.2396T>G	XP_011534554.1:p.Ile799Ser
NM_001350339.1:c.2081T>G	NP_001337268.1:p.Ile694Ser
NM_001350340.1:c.2081T>G	NP_001337269.1:p.Ile694Ser
NM_001350392.1:c.1556T>G	NP_001337321.1:p.Ile519Ser
XM_006715603.3:c.2396T>G	XP_006715666.1:p.Ile799Ser
XM_011536252.2:c.2396T>G	XP_011534554.1:p.Ile799Ser
XM_017011474.1:c.2396T>G	XP_016866963.1:p.Ile799Ser
XM_017011477.1:c.2396T>G	XP_016866966.1:p.Ile799Ser
XM_017011479.1:c.2396T>G	XP_016866968.1:p.Ile799Ser
XM_017011480.1:c.1556T>G	XP_016866969.1:p.Ile519Ser
XM_024446583.1:c.2396T>G	XP_024302351.1:p.Ile799Ser
NM_004690.4:c.2396T>G MANE Select	NP_004681.1:p.Ile799Ser
NM_001350339.2:c.2081T>G	NP_001337268.1:p.Ile694Ser
NM_001350340.2:c.2081T>G	NP_001337269.1:p.Ile694Ser
NM_001350392.2:c.1556T>G	NP_001337321.1:p.Ile519Ser
NR_073033.2:n.2850T>G