Canonical Allele Identifier: CA1938612187

Gene: GFRA1

Linked Data

• dbSNP Id: rs1962382832

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.116183040C>T , CM000672.2:g.116183040C>T	GRCh38
NC_000010.10:g.117942552C>T , CM000672.1:g.117942552C>T	GRCh37
NC_000010.9:g.117932542C>T	NCBI36
NG_050620.1:g.95606G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369234.5:c.433+28591G>A	ENSP00000358237.4:n.433+28591G>A
ENST00000439649.8:c.419-57483G>A	ENSP00000393725.3:n.419-57483G>A
ENST00000682489.1:c.433+28591G>A	ENSP00000508164.1:n.433+28591G>A
ENST00000682724.1:n.163-57483G>A
ENST00000682743.1:c.419-57483G>A	ENSP00000507970.1:n.419-57483G>A
ENST00000684105.1:c.419-57483G>A	ENSP00000506818.1:n.419-57483G>A
ENST00000355422.11:c.433+28591G>A MANE Select	ENSP00000347591.6:n.433+28591G>A
ENST00000355422.10:c.433+28591G>A	ENSP00000347591.6:n.433+28591G>A
ENST00000369234.4:c.433+28591G>A	ENSP00000358237.4:n.433+28591G>A
ENST00000369236.5:c.419-57483G>A	ENSP00000358239.1:n.419-57483G>A
ENST00000439649.7:c.419-57483G>A	ENSP00000393725.3:n.419-57483G>A
NM_001145453.1:c.419-57483G>A	NP_001138925.1:n.419-57483G>A
NM_005264.4:c.433+28591G>A	NP_005255.1:n.433+28591G>A
NM_145793.3:c.419-57483G>A	NP_665736.1:n.419-57483G>A
XM_005269696.1:c.433+28591G>A	XP_005269753.1:n.433+28591G>A
XM_011539634.1:c.433+28591G>A	XP_011537936.1:n.433+28591G>A
NM_001145453.2:c.419-57483G>A	NP_001138925.1:n.419-57483G>A
NM_001348096.1:c.419-57483G>A	NP_001335025.1:n.419-57483G>A
NM_001348098.1:c.433+28591G>A	NP_001335027.1:n.433+28591G>A
NM_001348099.1:c.71-57483G>A	NP_001335028.1:n.71-57483G>A
NM_005264.5:c.433+28591G>A	NP_005255.1:n.433+28591G>A
NM_145793.4:c.419-57483G>A	NP_665736.1:n.419-57483G>A
XM_011539634.2:c.433+28591G>A	XP_011537936.1:n.433+28591G>A
NM_001348098.2:c.433+28591G>A	NP_001335027.1:n.433+28591G>A
NM_005264.6:c.433+28591G>A	NP_005255.1:n.433+28591G>A
NM_145793.5:c.419-57483G>A	NP_665736.1:n.419-57483G>A
NM_001145453.4:c.419-57483G>A	NP_001138925.1:n.419-57483G>A
NM_001348096.3:c.419-57483G>A	NP_001335025.1:n.419-57483G>A
NM_001348098.4:c.433+28591G>A	NP_001335027.1:n.433+28591G>A
NM_001348099.3:c.71-57483G>A	NP_001335028.1:n.71-57483G>A
NM_001382556.2:c.419-57483G>A	NP_001369485.1:n.419-57483G>A
NM_001382557.2:c.419-57483G>A	NP_001369486.1:n.419-57483G>A
NM_001382558.2:c.419-57483G>A	NP_001369487.1:n.419-57483G>A
NM_001382559.2:c.419-57483G>A	NP_001369488.1:n.419-57483G>A
NM_001382560.2:c.419-57483G>A	NP_001369489.1:n.419-57483G>A
NM_001382561.2:c.419-57483G>A	NP_001369490.1:n.419-57483G>A
NM_005264.8:c.433+28591G>A MANE Select	NP_005255.1:n.433+28591G>A
NM_145793.7:c.419-57483G>A	NP_665736.1:n.419-57483G>A