Canonical Allele Identifier: CA339013881

Gene: GALE

Linked Data

• gnomAD v4: 1-23798180-C-A
• MyVariant Identifiers: chr1:g.24124670C>A (hg19) ; chr1:g.23798180C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798180C>A , CM000663.2:g.23798180C>A	GRCh38
NC_000001.10:g.24124670C>A , CM000663.1:g.24124670C>A	GRCh37
NC_000001.9:g.23997257C>A	NCBI36
NG_007068.1:g.7625G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.288G>T MANE Select	ENSP00000483375.1:p.Glu96Asp
ENST00000374497.7:c.288G>T	ENSP00000363621.3:p.Glu96Asp
ENST00000418277.5:c.96G>T	ENSP00000414719.1:p.Glu32Asp
ENST00000425913.5:c.288G>T	ENSP00000393359.1:p.Glu96Asp
ENST00000429356.5:c.96G>T	ENSP00000398585.1:p.Glu32Asp
ENST00000445705.1:c.288G>T	ENSP00000398257.1:p.Glu96Asp
ENST00000459934.5:n.406G>T
ENST00000467493.5:n.748G>T
ENST00000470949.5:n.233G>T
ENST00000481736.5:n.692G>T
ENST00000486382.1:n.389G>T
ENST00000617979.4:c.288G>T	ENSP00000483375.1:p.Glu96Asp
NM_000403.3:c.288G>T	NP_000394.2:p.Glu96Asp
NM_001008216.1:c.288G>T	NP_001008217.1:p.Glu96Asp
NM_001127621.1:c.288G>T	NP_001121093.1:p.Glu96Asp
NM_001008216.2:c.288G>T MANE Select	NP_001008217.1:p.Glu96Asp
NM_000403.4:c.288G>T	NP_000394.2:p.Glu96Asp
NM_001127621.2:c.288G>T	NP_001121093.1:p.Glu96Asp