Canonical Allele Identifier: CA353677857

Gene: ARL13B

Linked Data

• MyVariant Identifiers: chr3:g.93754177T>C (hg19) ; chr3:g.94035333T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.94035333T>C , CM000665.2:g.94035333T>C	GRCh38
NC_000003.11:g.93754177T>C , CM000665.1:g.93754177T>C	GRCh37
NC_000003.10:g.95236867T>C	NCBI36
NG_017076.1:g.60195T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394222.8:c.383T>C MANE Select	ENSP00000377769.3:p.Leu128Ser
ENST00000486562.2:c.62T>C	ENSP00000505366.1:p.Leu21Ser
ENST00000679404.1:c.308T>C	ENSP00000505252.1:p.Leu103Ser
ENST00000679587.1:c.383T>C	ENSP00000505396.1:p.Leu128Ser
ENST00000679601.1:c.*235T>C	ENSP00000506200.1:n.*235T>C
ENST00000679607.1:c.-455T>C	ENSP00000505148.1:n.-455T>C
ENST00000679654.1:c.255T>C	ENSP00000505178.1:p.Val85=
ENST00000679657.1:c.-32-14073T>C	ENSP00000505494.1:n.-32-14073T>C
ENST00000679666.1:c.11T>C	ENSP00000506469.1:p.Leu4Ser
ENST00000679739.1:c.72-1219T>C	ENSP00000506703.1:n.72-1219T>C
ENST00000679872.1:c.332T>C	ENSP00000505607.1:p.Leu111Ser
ENST00000680414.1:c.*233-1219T>C	ENSP00000506063.1:n.*233-1219T>C
ENST00000680430.1:c.632T>C	ENSP00000504943.1:n.632T>C
ENST00000680994.1:n.413T>C
ENST00000681013.1:c.381-1219T>C	ENSP00000506243.1:n.381-1219T>C
ENST00000681247.1:c.60-1219T>C	ENSP00000505168.1:n.60-1219T>C
ENST00000681380.1:c.383T>C	ENSP00000505402.1:p.Leu128Ser
ENST00000681655.1:c.308T>C	ENSP00000505036.1:p.Leu103Ser
ENST00000303097.11:c.62T>C	ENSP00000306225.7:p.Leu21Ser
ENST00000335438.7:c.*235T>C	ENSP00000335400.3:n.*235T>C
ENST00000394222.7:c.383T>C	ENSP00000377769.3:p.Leu128Ser
ENST00000460371.5:c.131-1219T>C	ENSP00000417263.1:n.131-1219T>C
ENST00000471138.5:c.383T>C	ENSP00000420780.1:p.Leu128Ser
ENST00000486562.1:n.339T>C
ENST00000535334.5:c.74T>C	ENSP00000445145.1:p.Leu25Ser
NM_001174150.1:c.383T>C	NP_001167621.1:p.Leu128Ser
NM_001174151.1:c.74T>C	NP_001167622.1:p.Leu25Ser
NM_144996.3:c.62T>C	NP_659433.2:p.Leu21Ser
NM_182896.2:c.383T>C	NP_878899.1:p.Leu128Ser
NR_033427.1:n.418T>C
XM_006713531.2:c.338T>C	XP_006713594.1:p.Leu113Ser
XM_006713532.2:c.338T>C	XP_006713595.1:p.Leu113Ser
XM_011512532.1:c.347T>C	XP_011510834.1:p.Leu116Ser
XM_011512533.1:c.347T>C	XP_011510835.1:p.Leu116Ser
XM_011512534.1:c.338T>C	XP_011510836.1:p.Leu113Ser
XM_011512535.1:c.308T>C	XP_011510837.1:p.Leu103Ser
XM_011512536.1:c.74T>C	XP_011510838.1:p.Leu25Ser
NM_001321328.1:c.338T>C	NP_001308257.1:p.Leu113Ser
NR_135621.1:n.414T>C
XM_006713532.3:c.338T>C	XP_006713595.1:p.Leu113Ser
XM_011512532.2:c.347T>C	XP_011510834.1:p.Leu116Ser
XM_011512533.2:c.347T>C	XP_011510835.1:p.Leu116Ser
XM_011512534.2:c.338T>C	XP_011510836.1:p.Leu113Ser
XM_011512535.2:c.308T>C	XP_011510837.1:p.Leu103Ser
XM_017005853.1:c.74T>C	XP_016861342.1:p.Leu25Ser
NM_001174150.2:c.383T>C MANE Select	NP_001167621.1:p.Leu128Ser
NM_001321328.2:c.338T>C	NP_001308257.1:p.Leu113Ser
NM_144996.4:c.62T>C	NP_659433.2:p.Leu21Ser
NM_182896.3:c.383T>C	NP_878899.1:p.Leu128Ser
NR_033427.2:n.402T>C
NR_135621.2:n.398T>C
NM_001174151.2:c.74T>C	NP_001167622.1:p.Leu25Ser