Canonical Allele Identifier: CA1845636648

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647710_34647712delinsCTA , CM000671.2:g.34647710_34647712delinsCTA	GRCh38
NC_000009.11:g.34647707_34647709delinsCTA , CM000671.1:g.34647707_34647709delinsCTA	GRCh37
NC_000009.10:g.34637707_34637709delinsCTA	NCBI36
NG_009029.1:g.6073_6075delinsCTA
NG_028966.1:g.526_528delinsCTA
NG_009029.2:g.6122_6124delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.329-122_329-120delinsCTA	ENSP00000509954.1:n.329-122_329-120delinsCTA
ENST00000378842.8:c.377+5_377+7delinsCTA MANE Select	ENSP00000368119.4:n.377+5_377+7delinsCTA
ENST00000378842.7:c.377+5_377+7delinsCTA	ENSP00000368119.3:n.377+5_377+7delinsCTA
ENST00000450095.6:c.51-122_51-120delinsCTA	ENSP00000401956.2:n.51-122_51-120delinsCTA
ENST00000465543.6:n.716+5_716+7delinsCTA
ENST00000472111.5:n.512_514delinsCTA
ENST00000473506.6:c.328+5_328+7delinsCTA	ENSP00000432839.2:n.328+5_328+7delinsCTA
ENST00000473529.5:n.513+5_513+7delinsCTA
ENST00000485531.1:n.697_699delinsCTA
ENST00000487381.5:n.641_643delinsCTA
ENST00000489643.6:n.283-405_283-403delinsCTA
ENST00000554085.5:c.*121+5_*121+7delinsCTA	ENSP00000450419.1:n.*121+5_*121+7delinsCTA
ENST00000554139.5:n.435_437delinsCTA
ENST00000554330.5:n.419_421delinsCTA
ENST00000554550.5:c.253-122_253-120delinsCTA	ENSP00000451435.1:n.253-122_253-120delinsCTA
ENST00000554638.5:n.728_730delinsCTA
ENST00000554897.5:c.253-122_253-120delinsCTA	ENSP00000450942.1:n.253-122_253-120delinsCTA
ENST00000554944.5:n.452_454delinsCTA
ENST00000555020.5:n.412_414delinsCTA
ENST00000555086.5:n.381+5_381+7delinsCTA
ENST00000555214.5:n.262-338_262-336delinsCTA
ENST00000556157.1:n.506_508delinsCTA
ENST00000556244.1:c.364+5_364+7delinsCTA
ENST00000556278.1:c.253-405_253-403delinsCTA	ENSP00000451792.1:n.253-405_253-403delinsCTA
ENST00000556403.5:n.484_486delinsCTA
ENST00000556494.5:n.498+5_498+7delinsCTA
ENST00000557541.5:n.521+5_521+7delinsCTA
ENST00000557706.5:n.818_820delinsCTA
NM_000155.3:c.377+5_377+7delinsCTA	NP_000146.2:n.377+5_377+7delinsCTA
NM_001258332.1:c.51-122_51-120delinsCTA	NP_001245261.1:n.51-122_51-120delinsCTA
NM_000155.4:c.377+5_377+7delinsCTA MANE Select	NP_000146.2:n.377+5_377+7delinsCTA
NM_001258332.2:c.51-122_51-120delinsCTA	NP_001245261.1:n.51-122_51-120delinsCTA