Canonical Allele Identifier: CA1845636036

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647439A= , CM000671.2:g.34647439A=	GRCh38
NC_000009.11:g.34647436A= , CM000671.1:g.34647436A=	GRCh37
NC_000009.10:g.34637436A=	NCBI36
NG_009029.1:g.5802A=
NG_028966.1:g.255A=
NG_009029.2:g.5851A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.253-53A=	ENSP00000509954.1:n.253-53A=
ENST00000378842.8:c.253-53A= MANE Select	ENSP00000368119.4:n.253-53A=
ENST00000378842.7:c.253-53A=	ENSP00000368119.3:n.253-53A=
ENST00000450095.6:c.50+181A=	ENSP00000401956.2:n.50+181A=
ENST00000465543.6:n.592-53A=
ENST00000468099.2:n.473A=
ENST00000472111.5:n.294-53A=
ENST00000473506.6:c.253-102A=	ENSP00000432839.2:n.253-102A=
ENST00000473529.5:n.300-53A=
ENST00000485531.1:n.426A=
ENST00000487381.5:n.459A=
ENST00000489643.6:n.282+181A=
ENST00000554085.5:c.253-36A=	ENSP00000450419.1:n.253-36A=
ENST00000554139.5:n.306-53A=
ENST00000554330.5:n.250-102A=
ENST00000554550.5:c.252+181A=	ENSP00000451435.1:n.252+181A=
ENST00000554638.5:n.457A=
ENST00000554897.5:c.252+181A=	ENSP00000450942.1:n.252+181A=
ENST00000554944.5:n.283-102A=
ENST00000555020.5:n.283-53A=
ENST00000555086.5:n.257-53A=
ENST00000555214.5:n.261+181A=
ENST00000556157.1:n.360-36A=
ENST00000556244.1:c.187A=
ENST00000556278.1:c.252+181A=	ENSP00000451792.1:n.252+181A=
ENST00000556403.5:n.266-53A=
ENST00000556494.5:n.285-53A=
ENST00000557541.5:n.446-102A=
ENST00000557706.5:n.547A=
NM_000155.3:c.253-53A=	NP_000146.2:n.253-53A=
NM_001258332.1:c.50+181A=	NP_001245261.1:n.50+181A=
NM_000155.4:c.253-53A= MANE Select	NP_000146.2:n.253-53A=
NM_001258332.2:c.50+181A=	NP_001245261.1:n.50+181A=