Canonical Allele Identifier: CA2627716066
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38349573_38349574insAAC , CM000677.2:g.38349573_38349574insAAC GRCh38
NC_000015.9:g.38641774_38641775insAAC , CM000677.1:g.38641774_38641775insAAC GRCh37
NC_000015.8:g.36429066_36429067insAAC NCBI36
NG_008980.1:g.101723_101724insAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.684+50_684+51insAAC MANE Select ENSP00000299084.4:n.684+50_684+51insAAC
ENST00000299084.8:c.684+50_684+51insAAC ENSP00000299084.4:n.684+50_684+51insAAC
NM_152594.2:c.684+50_684+51insAAC NP_689807.1:n.684+50_684+51insAAC
XM_005254202.2:c.720+50_720+51insAAC XP_005254259.1:n.720+50_720+51insAAC
XM_005254203.3:c.462+50_462+51insAAC XP_005254260.1:n.462+50_462+51insAAC
XM_011521288.1:c.621+50_621+51insAAC XP_011519590.1:n.621+50_621+51insAAC
XM_011521289.1:c.621+50_621+51insAAC XP_011519591.1:n.621+50_621+51insAAC
XM_011521290.1:c.621+50_621+51insAAC XP_011519592.1:n.621+50_621+51insAAC
XM_005254202.3:c.720+50_720+51insAAC XP_005254259.1:n.720+50_720+51insAAC
XM_011521289.3:c.621+50_621+51insAAC XP_011519591.1:n.621+50_621+51insAAC
NM_152594.3:c.684+50_684+51insAAC MANE Select NP_689807.1:n.684+50_684+51insAAC