Canonical Allele Identifier: CA2644079308

Gene: GALE

Linked Data

• gnomAD v4: 1-23798281-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798281A>G , CM000663.2:g.23798281A>G	GRCh38
NC_000001.10:g.24124771A>G , CM000663.1:g.24124771A>G	GRCh37
NC_000001.9:g.23997358A>G	NCBI36
NG_007068.1:g.7524T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.238-51T>C MANE Select	ENSP00000483375.1:n.238-51T>C
ENST00000374497.7:c.238-51T>C	ENSP00000363621.3:n.238-51T>C
ENST00000418277.5:c.46-51T>C	ENSP00000414719.1:n.46-51T>C
ENST00000425913.5:c.238-51T>C	ENSP00000393359.1:n.238-51T>C
ENST00000429356.5:c.46-51T>C	ENSP00000398585.1:n.46-51T>C
ENST00000445705.1:c.238-51T>C	ENSP00000398257.1:n.238-51T>C
ENST00000459934.5:n.356-51T>C
ENST00000467493.5:n.647T>C
ENST00000470949.5:n.188-56T>C
ENST00000481736.5:n.591T>C
ENST00000486382.1:n.344-56T>C
ENST00000617979.4:c.238-51T>C	ENSP00000483375.1:n.238-51T>C
NM_000403.3:c.238-51T>C	NP_000394.2:n.238-51T>C
NM_001008216.1:c.238-51T>C	NP_001008217.1:n.238-51T>C
NM_001127621.1:c.238-51T>C	NP_001121093.1:n.238-51T>C
NM_001008216.2:c.238-51T>C MANE Select	NP_001008217.1:n.238-51T>C
NM_000403.4:c.238-51T>C	NP_000394.2:n.238-51T>C
NM_001127621.2:c.238-51T>C	NP_001121093.1:n.238-51T>C