Canonical Allele Identifier: CA10605194

Gene: ARL13B

Linked Data

• ClinVar Variation Id: 285657
• ClinVar RCV Id: RCV000390849 ; RCV001378018
• dbSNP Id: rs373604132
• COSMIC: COSM4663322
• MyVariant Identifiers: chr3:g.93722502G>T (hg19) ; chr3:g.94003658G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.94003658G>T , CM000665.2:g.94003658G>T	GRCh38
NC_000003.11:g.93722502G>T , CM000665.1:g.93722502G>T	GRCh37
NC_000003.10:g.95205192G>T	NCBI36
NG_017076.1:g.28520G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394222.8:c.131-1G>T MANE Select	ENSP00000377769.3:n.131-1G>T
ENST00000475206.3:n.363-1G>T
ENST00000486562.2:c.59+23176G>T	ENSP00000505366.1:n.59+23176G>T
ENST00000492165.3:n.413-1G>T
ENST00000679404.1:c.56-1G>T	ENSP00000505252.1:n.56-1G>T
ENST00000679587.1:c.131-1G>T	ENSP00000505396.1:n.131-1G>T
ENST00000679601.1:c.268-1G>T	ENSP00000506200.1:n.268-1G>T
ENST00000679607.1:c.-458+14947G>T	ENSP00000505148.1:n.-458+14947G>T
ENST00000679654.1:c.252+6974G>T	ENSP00000505178.1:n.252+6974G>T
ENST00000679657.1:c.-33+23176G>T	ENSP00000505494.1:n.-33+23176G>T
ENST00000679666.1:c.8+14542G>T	ENSP00000506469.1:n.8+14542G>T
ENST00000679739.1:c.-179-1G>T	ENSP00000506703.1:n.-179-1G>T
ENST00000679872.1:c.80-1G>T	ENSP00000505607.1:n.80-1G>T
ENST00000680414.1:c.268-1G>T	ENSP00000506063.1:n.268-1G>T
ENST00000680430.1:c.380-1G>T	ENSP00000504943.1:n.380-1G>T
ENST00000680994.1:n.410+7714G>T
ENST00000681013.1:c.131-1G>T	ENSP00000506243.1:n.131-1G>T
ENST00000681247.1:c.59+23176G>T	ENSP00000505168.1:n.59+23176G>T
ENST00000681380.1:c.131-1G>T	ENSP00000505402.1:n.131-1G>T
ENST00000681655.1:c.56-1G>T	ENSP00000505036.1:n.56-1G>T
ENST00000303097.11:c.59+23176G>T	ENSP00000306225.7:n.59+23176G>T
ENST00000335438.7:c.253-1G>T	ENSP00000335400.3:n.253-1G>T
ENST00000394222.7:c.131-1G>T	ENSP00000377769.3:n.131-1G>T
ENST00000460371.5:c.130+7714G>T	ENSP00000417263.1:n.130+7714G>T
ENST00000471138.5:c.131-1G>T	ENSP00000420780.1:n.131-1G>T
ENST00000475206.2:n.422-1G>T
ENST00000486562.1:n.336+7714G>T
ENST00000492165.2:n.196-1G>T
ENST00000535334.5:c.-179-1G>T	ENSP00000445145.1:n.-179-1G>T
NM_001174150.1:c.131-1G>T	NP_001167621.1:n.131-1G>T
NM_001174151.1:c.-179-1G>T	NP_001167622.1:n.-179-1G>T
NM_144996.3:c.59+23176G>T	NP_659433.2:n.59+23176G>T
NM_182896.2:c.131-1G>T	NP_878899.1:n.131-1G>T
NR_033427.1:n.415+7714G>T
XM_006713531.2:c.86-1G>T	XP_006713594.1:n.86-1G>T
XM_006713532.2:c.86-1G>T	XP_006713595.1:n.86-1G>T
XM_011512532.1:c.95-1G>T	XP_011510834.1:n.95-1G>T
XM_011512533.1:c.95-1G>T	XP_011510835.1:n.95-1G>T
XM_011512534.1:c.86-1G>T	XP_011510836.1:n.86-1G>T
XM_011512535.1:c.56-1G>T	XP_011510837.1:n.56-1G>T
XM_011512536.1:c.-179-1G>T	XP_011510838.1:n.-179-1G>T
NM_001321328.1:c.86-1G>T	NP_001308257.1:n.86-1G>T
NR_135621.1:n.411+7714G>T
XM_006713532.3:c.86-1G>T	XP_006713595.1:n.86-1G>T
XM_011512532.2:c.95-1G>T	XP_011510834.1:n.95-1G>T
XM_011512533.2:c.95-1G>T	XP_011510835.1:n.95-1G>T
XM_011512534.2:c.86-1G>T	XP_011510836.1:n.86-1G>T
XM_011512535.2:c.56-1G>T	XP_011510837.1:n.56-1G>T
XM_017005853.1:c.-179-1G>T	XP_016861342.1:n.-179-1G>T
NM_001174150.2:c.131-1G>T MANE Select	NP_001167621.1:n.131-1G>T
NM_001321328.2:c.86-1G>T	NP_001308257.1:n.86-1G>T
NM_144996.4:c.59+23176G>T	NP_659433.2:n.59+23176G>T
NM_182896.3:c.131-1G>T	NP_878899.1:n.131-1G>T
NR_033427.2:n.399+7714G>T
NR_135621.2:n.395+7714G>T
NM_001174151.2:c.-179-1G>T	NP_001167622.1:n.-179-1G>T