Canonical Allele Identifier: CA2170799283
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38322172T= , CM000677.2:g.38322172T= GRCh38
NC_000015.9:g.38614373T= , CM000677.1:g.38614373T= GRCh37
NC_000015.8:g.36401665T= NCBI36
NG_008980.1:g.74322T=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.208-69T= MANE Select ENSP00000299084.4:n.208-69T=
ENST00000299084.8:c.208-69T= ENSP00000299084.4:n.208-69T=
ENST00000561205.1:n.546-69T=
ENST00000561317.1:c.145-69T= ENSP00000453680.1:n.145-69T=
NM_152594.2:c.208-69T= NP_689807.1:n.208-69T=
XM_005254202.2:c.244-69T= XP_005254259.1:n.244-69T=
XM_005254203.3:c.-15-69T= XP_005254260.1:n.-15-69T=
XM_011521288.1:c.145-69T= XP_011519590.1:n.145-69T=
XM_011521289.1:c.145-69T= XP_011519591.1:n.145-69T=
XM_011521290.1:c.145-69T= XP_011519592.1:n.145-69T=
XM_005254202.3:c.244-69T= XP_005254259.1:n.244-69T=
XM_011521289.3:c.145-69T= XP_011519591.1:n.145-69T=
NM_152594.3:c.208-69T= MANE Select NP_689807.1:n.208-69T=