Canonical Allele Identifier: CA339006904

Gene: GALE

Linked Data

• MyVariant Identifiers: chr1:g.24123078T>G (hg19) ; chr1:g.23796588T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23796588T>G , CM000663.2:g.23796588T>G	GRCh38
NC_000001.10:g.24123078T>G , CM000663.1:g.24123078T>G	GRCh37
NC_000001.9:g.23995665T>G	NCBI36
NG_007068.1:g.9217A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.796-2A>C MANE Select	ENSP00000483375.1:n.796-2A>C
ENST00000374497.7:c.796-2A>C	ENSP00000363621.3:n.796-2A>C
ENST00000418277.5:c.604-2A>C	ENSP00000414719.1:n.604-2A>C
ENST00000429356.5:c.603+109A>C	ENSP00000398585.1:n.603+109A>C
ENST00000456977.5:c.153+109A>C	ENSP00000397045.1:n.153+109A>C
ENST00000459934.5:n.1022A>C
ENST00000469556.1:n.298A>C
ENST00000481736.5:n.1200-2A>C
ENST00000617979.4:c.796-2A>C	ENSP00000483375.1:n.796-2A>C
NM_000403.3:c.796-2A>C	NP_000394.2:n.796-2A>C
NM_001008216.1:c.796-2A>C	NP_001008217.1:n.796-2A>C
NM_001127621.1:c.796-2A>C	NP_001121093.1:n.796-2A>C
NM_001008216.2:c.796-2A>C MANE Select	NP_001008217.1:n.796-2A>C
NM_000403.4:c.796-2A>C	NP_000394.2:n.796-2A>C
NM_001127621.2:c.796-2A>C	NP_001121093.1:n.796-2A>C