Canonical Allele Identifier: CA2170812863

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351786_38351787delinsAG , CM000677.2:g.38351786_38351787delinsAG	GRCh38
NC_000015.9:g.38643987_38643988delinsAG , CM000677.1:g.38643987_38643988delinsAG	GRCh37
NC_000015.8:g.36431279_36431280delinsAG	NCBI36
NG_008980.1:g.103936_103937delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*122_*123delinsAG MANE Select	ENSP00000299084.4:n.*122_*123delinsAG
ENST00000299084.8:c.*122_*123delinsAG	ENSP00000299084.4:n.*122_*123delinsAG
NM_152594.2:c.*122_*123delinsAG	NP_689807.1:n.*122_*123delinsAG
XM_005254202.2:c.*122_*123delinsAG	XP_005254259.1:n.*122_*123delinsAG
XM_005254203.3:c.*122_*123delinsAG	XP_005254260.1:n.*122_*123delinsAG
XM_011521288.1:c.*122_*123delinsAG	XP_011519590.1:n.*122_*123delinsAG
XM_011521289.1:c.*122_*123delinsAG	XP_011519591.1:n.*122_*123delinsAG
XM_011521290.1:c.*122_*123delinsAG	XP_011519592.1:n.*122_*123delinsAG
XM_005254202.3:c.*122_*123delinsAG	XP_005254259.1:n.*122_*123delinsAG
XM_011521289.3:c.*122_*123delinsAG	XP_011519591.1:n.*122_*123delinsAG
NM_152594.3:c.*122_*123delinsAG MANE Select	NP_689807.1:n.*122_*123delinsAG