Canonical Allele Identifier: CA1845636567

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647685_34647698delinsAAAGTCTGCTCGAG , CM000671.2:g.34647685_34647698delinsAAAGTCTGCTCGAG	GRCh38
NC_000009.11:g.34647682_34647695delinsAAAGTCTGCTCGAG , CM000671.1:g.34647682_34647695delinsAAAGTCTGCTCGAG	GRCh37
NC_000009.10:g.34637682_34637695delinsAAAGTCTGCTCGAG	NCBI36
NG_009029.1:g.6048_6061delinsAAAGTCTGCTCGAG
NG_028966.1:g.501_514delinsAAAGTCTGCTCGAG
NG_009029.2:g.6097_6110delinsAAAGTCTGCTCGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.328+118_328+131delinsAAAGTCTGCTCGAG	ENSP00000509954.1:n.328+118_328+131delinsAAAGTCTGCTCGAG
ENST00000378842.8:c.357_370delinsAAAGTCTGCTCGAG MANE Select	ENSP00000368119.4:p.Ala119=
ENST00000378842.7:c.357_370delinsAAAGTCTGCTCGAG	ENSP00000368119.3:p.Ala119=
ENST00000450095.6:c.51-147_51-134delinsAAAGTCTGCTCGAG	ENSP00000401956.2:n.51-147_51-134delinsAAAGTCTGCTCGAG
ENST00000465543.6:n.696_709delinsAAAGTCTGCTCGAG
ENST00000472111.5:n.487_500delinsAAAGTCTGCTCGAG
ENST00000473506.6:c.308_321delinsAAAGTCTGCTCGAG	ENSP00000432839.2:p.Gln103=
ENST00000473529.5:n.493_506delinsAAAGTCTGCTCGAG
ENST00000485531.1:n.672_685delinsAAAGTCTGCTCGAG
ENST00000487381.5:n.616_629delinsAAAGTCTGCTCGAG
ENST00000489643.6:n.282+427_283-417delinsAAAGTCTGCTCGAG
ENST00000554085.5:c.*101_*114delinsAAAGTCTGCTCGAG	ENSP00000450419.1:n.*101_*114delinsAAAGTCTGCTCGAG
ENST00000554139.5:n.410_423delinsAAAGTCTGCTCGAG
ENST00000554330.5:n.394_407delinsAAAGTCTGCTCGAG
ENST00000554550.5:c.253-147_253-134delinsAAAGTCTGCTCGAG	ENSP00000451435.1:n.253-147_253-134delinsAAAGTCTGCTCGAG
ENST00000554638.5:n.703_716delinsAAAGTCTGCTCGAG
ENST00000554897.5:c.253-147_253-134delinsAAAGTCTGCTCGAG	ENSP00000450942.1:n.253-147_253-134delinsAAAGTCTGCTCGAG
ENST00000554944.5:n.427_440delinsAAAGTCTGCTCGAG
ENST00000555020.5:n.387_400delinsAAAGTCTGCTCGAG
ENST00000555086.5:n.361_374delinsAAAGTCTGCTCGAG
ENST00000555214.5:n.262-363_262-350delinsAAAGTCTGCTCGAG
ENST00000556157.1:n.481_494delinsAAAGTCTGCTCGAG
ENST00000556244.1:c.344_357delinsAAAGTCTGCTCGAG
ENST00000556278.1:c.252+427_253-417delinsAAAGTCTGCTCGAG	ENSP00000451792.1:n.252+427_253-417delinsAAAGTCTGCTCGAG
ENST00000556403.5:n.459_472delinsAAAGTCTGCTCGAG
ENST00000556494.5:n.478_491delinsAAAGTCTGCTCGAG
ENST00000557541.5:n.501_514delinsAAAGTCTGCTCGAG
ENST00000557706.5:n.793_806delinsAAAGTCTGCTCGAG
NM_000155.3:c.357_370delinsAAAGTCTGCTCGAG	NP_000146.2:p.Ala119=
NM_001258332.1:c.51-147_51-134delinsAAAGTCTGCTCGAG	NP_001245261.1:n.51-147_51-134delinsAAAGTCTGCTCGAG
NM_000155.4:c.357_370delinsAAAGTCTGCTCGAG MANE Select	NP_000146.2:p.Ala119=
NM_001258332.2:c.51-147_51-134delinsAAAGTCTGCTCGAG	NP_001245261.1:n.51-147_51-134delinsAAAGTCTGCTCGAG