Canonical Allele Identifier: CA898599384

Gene: MGLL

Linked Data

• dbSNP Id: rs1237592877
• MyVariant Identifiers: chr3:g.127473954del (hg19) ; chr3:g.127755111del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.127755113del , CM000665.2:g.127755113del	GRCh38
NC_000003.11:g.127473956del , CM000665.1:g.127473956del	GRCh37
NC_000003.10:g.128956646del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265052.10:c.262+26678del MANE Select	ENSP00000265052.5:n.262+26678del
ENST00000398104.6:c.232+26678del	ENSP00000381176.1:n.232+26678del
ENST00000453507.7:c.262+26678del	ENSP00000404146.2:n.262+26678del
ENST00000487473.6:c.82+26678del	ENSP00000420125.2:n.82+26678del
ENST00000648300.1:c.232+26678del	ENSP00000497905.1:n.232+26678del
ENST00000265052.9:c.262+26678del	ENSP00000265052.5:n.262+26678del
ENST00000398104.5:c.232+26678del	ENSP00000381176.1:n.232+26678del
ENST00000434178.6:c.232+26678del	ENSP00000402798.2:n.232+26678del
ENST00000453507.6:c.262+26678del	ENSP00000404146.2:n.262+26678del
ENST00000465597.5:n.152+26678del
ENST00000476654.1:n.169+26678del
ENST00000479967.5:n.354+26678del
ENST00000493611.1:c.43+26678del	ENSP00000417689.1:n.43+26678del
NM_001003794.2:c.232+26678del	NP_001003794.1:n.232+26678del
NM_001256585.1:c.262+26678del	NP_001243514.1:n.262+26678del
NM_007283.6:c.262+26678del	NP_009214.1:n.262+26678del
XM_011512377.1:c.262+26678del	XP_011510679.1:n.262+26678del
XM_011512378.1:c.232+26678del	XP_011510680.1:n.232+26678del
XM_011512379.1:c.-35-19218del	XP_011510681.1:n.-35-19218del
XM_011512380.1:c.-35-19218del	XP_011510682.1:n.-35-19218del
XM_011512381.1:c.-35-19218del	XP_011510683.1:n.-35-19218del
XM_011512382.1:c.43+26678del	XP_011510684.1:n.43+26678del
XM_011512383.1:c.-35-19218del	XP_011510685.1:n.-35-19218del
XM_011512377.2:c.262+26678del	XP_011510679.1:n.262+26678del
XM_011512378.2:c.232+26678del	XP_011510680.1:n.232+26678del
XM_011512379.2:c.-35-19218del	XP_011510681.1:n.-35-19218del
XM_011512383.2:c.-35-19218del	XP_011510685.1:n.-35-19218del
XM_017005662.2:c.232+26678del	XP_016861151.1:n.232+26678del
XM_017005663.1:c.-35-19218del	XP_016861152.1:n.-35-19218del
XM_017005664.2:c.-35-19218del	XP_016861153.1:n.-35-19218del
XM_017005666.2:c.232+26678del	XP_016861155.1:n.232+26678del
XM_024453333.1:c.-35-19218del	XP_024309101.1:n.-35-19218del
XM_024453334.1:c.43+26678del	XP_024309102.1:n.43+26678del
NM_001003794.3:c.232+26678del	NP_001003794.1:n.232+26678del
NM_001256585.2:c.262+26678del	NP_001243514.1:n.262+26678del
NM_001388312.1:c.262+26678del	NP_001375241.1:n.262+26678del
NM_001388313.1:c.232+26678del	NP_001375242.1:n.232+26678del
NM_001388314.1:c.232+26678del	NP_001375243.1:n.232+26678del
NM_001388315.1:c.-35-19218del	NP_001375244.1:n.-35-19218del
NM_001388316.1:c.232+26678del	NP_001375245.1:n.232+26678del
NM_001388317.1:c.-35-19218del	NP_001375246.1:n.-35-19218del
NM_001388318.1:c.-35-19218del	NP_001375247.1:n.-35-19218del
NM_007283.7:c.262+26678del MANE Select	NP_009214.1:n.262+26678del