Canonical Allele Identifier: CA1845635989

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647401_34647402delinsCT , CM000671.2:g.34647401_34647402delinsCT	GRCh38
NC_000009.11:g.34647398_34647399delinsCT , CM000671.1:g.34647398_34647399delinsCT	GRCh37
NC_000009.10:g.34637398_34637399delinsCT	NCBI36
NG_009029.1:g.5764_5765delinsCT
NG_028966.1:g.217_218delinsCT
NG_009029.2:g.5813_5814delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.253-91_253-90delinsCT	ENSP00000509954.1:n.253-91_253-90delinsCT...
ENST00000378842.8:c.253-91_253-90delinsCT MANE Select	ENSP00000368119.4:n.253-91_253-90delinsCT...
ENST00000378842.7:c.253-91_253-90delinsCT	ENSP00000368119.3:n.253-91_253-90delinsCT...
ENST00000450095.6:c.50+143_50+144delinsCT	ENSP00000401956.2:n.50+143_50+144delinsCT...
ENST00000465543.6:n.592-91_592-90delinsCT
ENST00000468099.2:n.435_436delinsCT
ENST00000472111.5:n.294-91_294-90delinsCT
ENST00000473506.6:c.253-140_253-139delinsCT	ENSP00000432839.2:n.253-140_253-139delins...
ENST00000473529.5:n.300-91_300-90delinsCT
ENST00000485531.1:n.388_389delinsCT
ENST00000487381.5:n.421_422delinsCT
ENST00000489643.6:n.282+143_282+144delinsCT
ENST00000554085.5:c.253-74_253-73delinsCT	ENSP00000450419.1:n.253-74_253-73delinsCT...
ENST00000554139.5:n.306-91_306-90delinsCT
ENST00000554330.5:n.250-140_250-139delinsCT
ENST00000554550.5:c.252+143_252+144delinsCT	ENSP00000451435.1:n.252+143_252+144delins...
ENST00000554638.5:n.419_420delinsCT
ENST00000554897.5:c.252+143_252+144delinsCT	ENSP00000450942.1:n.252+143_252+144delins...
ENST00000554944.5:n.283-140_283-139delinsCT
ENST00000555020.5:n.283-91_283-90delinsCT
ENST00000555086.5:n.257-91_257-90delinsCT
ENST00000555214.5:n.261+143_261+144delinsCT
ENST00000556157.1:n.360-74_360-73delinsCT
ENST00000556244.1:c.149_150delinsCT
ENST00000556278.1:c.252+143_252+144delinsCT	ENSP00000451792.1:n.252+143_252+144delins...
ENST00000556403.5:n.266-91_266-90delinsCT
ENST00000556494.5:n.285-91_285-90delinsCT
ENST00000557541.5:n.446-140_446-139delinsCT
ENST00000557706.5:n.509_510delinsCT
NM_000155.3:c.253-91_253-90delinsCT	NP_000146.2:n.253-91_253-90delinsCT
NM_001258332.1:c.50+143_50+144delinsCT	NP_001245261.1:n.50+143_50+144delinsCT
NM_000155.4:c.253-91_253-90delinsCT MANE Select	NP_000146.2:n.253-91_253-90delinsCT
NM_001258332.2:c.50+143_50+144delinsCT	NP_001245261.1:n.50+143_50+144delinsCT