Canonical Allele Identifier: CA339015638

Gene: GALE

Linked Data

• dbSNP Id: rs121908046
• gnomAD v4: 1-23798907-T-G
• MyVariant Identifiers: chr1:g.24125397T>G (hg19) ; chr1:g.23798907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23798907T>G , CM000663.2:g.23798907T>G	GRCh38
NC_000001.10:g.24125397T>G , CM000663.1:g.24125397T>G	GRCh37
NC_000001.9:g.23997984T>G	NCBI36
NG_007068.1:g.6898A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000617979.5:c.101A>C MANE Select	ENSP00000483375.1:p.Asn34Thr
ENST00000374497.7:c.101A>C	ENSP00000363621.3:p.Asn34Thr
ENST00000418277.5:c.-71-177A>C	ENSP00000414719.1:n.-71-177A>C
ENST00000425913.5:c.101A>C	ENSP00000393359.1:p.Asn34Thr
ENST00000429356.5:c.-71-177A>C	ENSP00000398585.1:n.-71-177A>C
ENST00000445705.1:c.101A>C	ENSP00000398257.1:p.Asn34Thr
ENST00000459934.5:n.219A>C
ENST00000466250.5:n.227A>C
ENST00000467070.1:n.499A>C
ENST00000467493.5:n.177A>C
ENST00000470383.1:n.1493A>C
ENST00000470949.5:n.72-177A>C
ENST00000481736.5:n.142-177A>C
ENST00000486382.1:n.207A>C
ENST00000617979.4:c.101A>C	ENSP00000483375.1:p.Asn34Thr
NM_000403.3:c.101A>C	NP_000394.2:p.Asn34Thr
NM_001008216.1:c.101A>C	NP_001008217.1:p.Asn34Thr
NM_001127621.1:c.101A>C	NP_001121093.1:p.Asn34Thr
NM_001008216.2:c.101A>C MANE Select	NP_001008217.1:p.Asn34Thr
NM_000403.4:c.101A>C	NP_000394.2:p.Asn34Thr
NM_001127621.2:c.101A>C	NP_001121093.1:p.Asn34Thr