Canonical Allele Identifier: CA405906527

Gene: LTBP4

Linked Data

• MyVariant Identifiers: chr19:g.41128486A>G (hg19) ; chr19:g.40622581A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40622581A>G , CM000681.2:g.40622581A>G	GRCh38
NC_000019.9:g.41128486A>G , CM000681.1:g.41128486A>G	GRCh37
NC_000019.8:g.45820326A>G	NCBI36
NG_021201.1:g.34416A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396819.8:c.3398A>G MANE Select	ENSP00000380031.5:p.Asn1133Ser
ENST00000204005.13:c.3488A>G	ENSP00000204005.10:p.Asn1163Ser
ENST00000243562.13:c.1597A>G
ENST00000308370.11:c.3599A>G	ENSP00000311905.8:p.Asn1200Ser
ENST00000318809.11:n.484-1023A>G
ENST00000396819.7:c.3398A>G	ENSP00000380031.4:p.Asn1133Ser
ENST00000593463.5:c.535-1023A>G
ENST00000594116.1:n.194A>G
ENST00000595118.5:n.903A>G
ENST00000595665.1:n.535-1023A>G
ENST00000597816.5:n.453-1023A>G
ENST00000599724.5:c.485-1023A>G	ENSP00000469785.1:n.485-1023A>G
ENST00000601032.5:c.1035A>G
ENST00000622107.4:n.545-1023A>G
ENST00000622457.1:c.385-1023A>G
ENST00000622565.4:n.727-1023A>G
NM_001042544.1:c.3599A>G	NP_001036009.1:p.Asn1200Ser
NM_001042545.1:c.3398A>G	NP_001036010.1:p.Asn1133Ser
NM_003573.2:c.3488A>G	NP_003564.2:p.Asn1163Ser
XM_011527376.1:c.3713A>G	XP_011525678.1:p.Asn1238Ser
XM_011527377.1:c.3632A>G	XP_011525679.1:p.Asn1211Ser
XM_011527378.1:c.3632A>G	XP_011525680.1:p.Asn1211Ser
XM_011527379.1:c.3512A>G	XP_011525681.1:p.Asn1171Ser
XM_011527380.1:c.3506A>G	XP_011525682.1:p.Asn1169Ser
XM_011527381.1:c.3506A>G	XP_011525683.1:p.Asn1169Ser
XM_011527382.1:c.3389A>G	XP_011525684.1:p.Asn1130Ser
XM_011527383.1:c.3452-1023A>G	XP_011525685.1:n.3452-1023A>G
XM_011527384.1:c.3326-1023A>G	XP_011525686.1:n.3326-1023A>G
XM_011527385.1:c.3320-1023A>G	XP_011525687.1:n.3320-1023A>G
XM_011527386.1:c.3194-1023A>G	XP_011525688.1:n.3194-1023A>G
XM_011527387.1:c.2990A>G	XP_011525689.1:p.Asn997Ser
XM_011527376.2:c.3713A>G	XP_011525678.1:p.Asn1238Ser
XM_011527377.2:c.3632A>G	XP_011525679.1:p.Asn1211Ser
XM_011527378.2:c.3632A>G	XP_011525680.1:p.Asn1211Ser
XM_011527380.2:c.3506A>G	XP_011525682.1:p.Asn1169Ser
XM_011527381.2:c.3506A>G	XP_011525683.1:p.Asn1169Ser
XM_011527382.2:c.3389A>G	XP_011525684.1:p.Asn1130Ser
XM_011527383.2:c.3452-1023A>G	XP_011525685.1:n.3452-1023A>G
XM_011527384.2:c.3326-1023A>G	XP_011525686.1:n.3326-1023A>G
XM_011527385.2:c.3320-1023A>G	XP_011525687.1:n.3320-1023A>G
XM_011527386.2:c.3194-1023A>G	XP_011525688.1:n.3194-1023A>G
XM_017027352.1:c.3500A>G	XP_016882841.1:p.Asn1167Ser
XM_017027353.1:c.3374A>G	XP_016882842.1:p.Asn1125Ser
XM_017027354.1:c.3200-1023A>G	XP_016882843.1:n.3200-1023A>G
NM_001042545.2:c.3398A>G MANE Select	NP_001036010.1:p.Asn1133Ser