Canonical Allele Identifier: CA13020526
Gene: GARNL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127345685A>G , CM000671.2:g.127345685A>G GRCh38
NC_000009.11:g.130107964A>G , CM000671.1:g.130107964A>G GRCh37
NC_000009.10:g.129147785A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000373387.9:c.1431+208A>G MANE Select ENSP00000362485.4:n.1431+208A>G
ENST00000373386.6:c.1377+208A>G ENSP00000362484.2:n.1377+208A>G
ENST00000373387.8:c.1431+208A>G ENSP00000362485.4:n.1431+208A>G
ENST00000435213.6:c.1365+208A>G ENSP00000396205.2:n.1365+208A>G
ENST00000460176.6:c.200+208A>G
NM_001286779.1:c.1365+208A>G NP_001273708.1:n.1365+208A>G
NM_032293.4:c.1431+208A>G NP_115669.3:n.1431+208A>G
NR_104591.1:n.1832+208A>G
XM_005252267.2:c.1620+208A>G XP_005252324.1:n.1620+208A>G
XM_005252268.1:c.1500+208A>G XP_005252325.1:n.1500+208A>G
XM_011519086.1:c.1578+208A>G XP_011517388.1:n.1578+208A>G
XM_011519087.1:c.1578+208A>G XP_011517389.1:n.1578+208A>G
XM_011519088.1:c.1578+208A>G XP_011517390.1:n.1578+208A>G
XM_011519089.1:c.1500+208A>G XP_011517391.1:n.1500+208A>G
XM_011519090.1:c.924+208A>G XP_011517392.1:n.924+208A>G
XM_005252267.3:c.1620+208A>G XP_005252324.1:n.1620+208A>G
XM_005252268.2:c.1500+208A>G XP_005252325.1:n.1500+208A>G
XM_011519086.3:c.1578+208A>G XP_011517388.1:n.1578+208A>G
XM_011519087.2:c.1578+208A>G XP_011517389.1:n.1578+208A>G
XM_011519089.3:c.1500+208A>G XP_011517391.1:n.1500+208A>G
XM_011519090.2:c.924+208A>G XP_011517392.1:n.924+208A>G
XM_017015202.1:c.1473+208A>G XP_016870691.1:n.1473+208A>G
XM_024447693.1:c.1500+208A>G XP_024303461.1:n.1500+208A>G
XM_024447694.1:c.924+208A>G XP_024303462.1:n.924+208A>G
XM_024447695.1:c.924+208A>G XP_024303463.1:n.924+208A>G
XM_024447696.1:c.924+208A>G XP_024303464.1:n.924+208A>G
XM_024447697.1:c.924+208A>G XP_024303465.1:n.924+208A>G
XR_001746389.1:n.1687+208A>G
NM_032293.5:c.1431+208A>G MANE Select NP_115669.3:n.1431+208A>G
NM_001286779.2:c.1365+208A>G NP_001273708.1:n.1365+208A>G
NR_104591.2:n.1535+208A>G