Canonical Allele Identifier: CA2627716312

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38351842-A-ACATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351842_38351843insCATTTT , CM000677.2:g.38351842_38351843insCATTTT	GRCh38
NC_000015.9:g.38644043_38644044insCATTTT , CM000677.1:g.38644043_38644044insCATTTT	GRCh37
NC_000015.8:g.36431335_36431336insCATTTT	NCBI36
NG_008980.1:g.103992_103993insCATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*178_*179insCATTTT MANE Select	ENSP00000299084.4:n.*178_*179insCATTTT
ENST00000299084.8:c.*178_*179insCATTTT	ENSP00000299084.4:n.*178_*179insCATTTT
NM_152594.2:c.*178_*179insCATTTT	NP_689807.1:n.*178_*179insCATTTT
XM_005254202.2:c.*178_*179insCATTTT	XP_005254259.1:n.*178_*179insCATTTT
XM_005254203.3:c.*178_*179insCATTTT	XP_005254260.1:n.*178_*179insCATTTT
XM_011521288.1:c.*178_*179insCATTTT	XP_011519590.1:n.*178_*179insCATTTT
XM_011521289.1:c.*178_*179insCATTTT	XP_011519591.1:n.*178_*179insCATTTT
XM_011521290.1:c.*178_*179insCATTTT	XP_011519592.1:n.*178_*179insCATTTT
XM_005254202.3:c.*178_*179insCATTTT	XP_005254259.1:n.*178_*179insCATTTT
XM_011521289.3:c.*178_*179insCATTTT	XP_011519591.1:n.*178_*179insCATTTT
NM_152594.3:c.*178_*179insCATTTT MANE Select	NP_689807.1:n.*178_*179insCATTTT