Canonical Allele Identifier: CA2695714206

Gene: GALE

Linked Data

• dbSNP Id: rs2148411325

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23797999del , CM000663.2:g.23797999del	GRCh38
NC_000001.10:g.24124489del , CM000663.1:g.24124489del	GRCh37
NC_000001.9:g.23997076del	NCBI36
NG_007068.1:g.7808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617979.5:c.351+120del MANE Select	ENSP00000483375.1:n.351+120del
ENST00000374497.7:c.351+120del	ENSP00000363621.3:n.351+120del
ENST00000418277.5:c.159+120del	ENSP00000414719.1:n.159+120del
ENST00000425913.5:c.351+120del	ENSP00000393359.1:n.351+120del
ENST00000429356.5:c.159+120del	ENSP00000398585.1:n.159+120del
ENST00000445705.1:c.351+120del	ENSP00000398257.1:n.351+120del
ENST00000459934.5:n.469+120del
ENST00000467493.5:n.811+120del
ENST00000470949.5:n.296+120del
ENST00000481736.5:n.755+120del
ENST00000617979.4:c.351+120del	ENSP00000483375.1:n.351+120del
NM_000403.3:c.351+120del	NP_000394.2:n.351+120del
NM_001008216.1:c.351+120del	NP_001008217.1:n.351+120del
NM_001127621.1:c.351+120del	NP_001121093.1:n.351+120del
NM_001008216.2:c.351+120del MANE Select	NP_001008217.1:n.351+120del
NM_000403.4:c.351+120del	NP_000394.2:n.351+120del
NM_001127621.2:c.351+120del	NP_001121093.1:n.351+120del