Canonical Allele Identifier: CA1845635728

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647223_34647225delinsCCT , CM000671.2:g.34647223_34647225delinsCCT	GRCh38
NC_000009.11:g.34647220_34647222delinsCCT , CM000671.1:g.34647220_34647222delinsCCT	GRCh37
NC_000009.10:g.34637220_34637222delinsCCT	NCBI36
NG_009029.1:g.5586_5588delinsCCT
NG_028966.1:g.39_41delinsCCT
NG_009029.2:g.5635_5637delinsCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.217_219delinsCCT	ENSP00000509954.1:p.Pro73=
ENST00000378842.8:c.217_219delinsCCT MANE Select	ENSP00000368119.4:p.Pro73=
ENST00000378842.7:c.217_219delinsCCT	ENSP00000368119.3:p.Pro73=
ENST00000450095.6:c.15_17delinsCCT	ENSP00000401956.2:p.Thr5=
ENST00000465543.6:n.556_558delinsCCT
ENST00000468099.2:n.257_259delinsCCT
ENST00000472111.5:n.258_260delinsCCT
ENST00000473506.6:c.217_219delinsCCT	ENSP00000432839.2:p.Pro73=
ENST00000473529.5:n.264_266delinsCCT
ENST00000485531.1:n.210_212delinsCCT
ENST00000487381.5:n.243_245delinsCCT
ENST00000489643.6:n.247_249delinsCCT
ENST00000554085.5:c.217_219delinsCCT	ENSP00000450419.1:p.Pro73=
ENST00000554139.5:n.270_272delinsCCT
ENST00000554330.5:n.214_216delinsCCT
ENST00000554550.5:c.217_219delinsCCT	ENSP00000451435.1:p.Pro73=
ENST00000554638.5:n.241_243delinsCCT
ENST00000554897.5:c.217_219delinsCCT	ENSP00000450942.1:p.Pro73=
ENST00000554944.5:n.247_249delinsCCT
ENST00000555020.5:n.247_249delinsCCT
ENST00000555086.5:n.221_223delinsCCT
ENST00000555214.5:n.226_228delinsCCT
ENST00000556157.1:n.324_326delinsCCT
ENST00000556244.1:c.101_103delinsCCT
ENST00000556278.1:c.217_219delinsCCT	ENSP00000451792.1:p.Pro73=
ENST00000556403.5:n.230_232delinsCCT
ENST00000556494.5:n.249_251delinsCCT
ENST00000557541.5:n.410_412delinsCCT
ENST00000557706.5:n.331_333delinsCCT
NM_000155.3:c.217_219delinsCCT	NP_000146.2:p.Pro73=
NM_001258332.1:c.15_17delinsCCT	NP_001245261.1:p.Thr5=
NM_000155.4:c.217_219delinsCCT MANE Select	NP_000146.2:p.Pro73=
NM_001258332.2:c.15_17delinsCCT	NP_001245261.1:p.Thr5=