Canonical Allele Identifier: CA339014124

Gene: GALE

Linked Data

• MyVariant Identifiers: chr1:g.24124696A>C (hg19) ; chr1:g.23798206A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798206A>C , CM000663.2:g.23798206A>C	GRCh38
NC_000001.10:g.24124696A>C , CM000663.1:g.24124696A>C	GRCh37
NC_000001.9:g.23997283A>C	NCBI36
NG_007068.1:g.7599T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.262T>G MANE Select	ENSP00000483375.1:p.Phe88Val
ENST00000374497.7:c.262T>G	ENSP00000363621.3:p.Phe88Val
ENST00000418277.5:c.70T>G	ENSP00000414719.1:p.Phe24Val
ENST00000425913.5:c.262T>G	ENSP00000393359.1:p.Phe88Val
ENST00000429356.5:c.70T>G	ENSP00000398585.1:p.Phe24Val
ENST00000445705.1:c.262T>G	ENSP00000398257.1:p.Phe88Val
ENST00000459934.5:n.380T>G
ENST00000467493.5:n.722T>G
ENST00000470949.5:n.207T>G
ENST00000481736.5:n.666T>G
ENST00000486382.1:n.363T>G
ENST00000617979.4:c.262T>G	ENSP00000483375.1:p.Phe88Val
NM_000403.3:c.262T>G	NP_000394.2:p.Phe88Val
NM_001008216.1:c.262T>G	NP_001008217.1:p.Phe88Val
NM_001127621.1:c.262T>G	NP_001121093.1:p.Phe88Val
NM_001008216.2:c.262T>G MANE Select	NP_001008217.1:p.Phe88Val
NM_000403.4:c.262T>G	NP_000394.2:p.Phe88Val
NM_001127621.2:c.262T>G	NP_001121093.1:p.Phe88Val