Canonical Allele Identifier: CA2575673202

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38322170-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322170T>C , CM000677.2:g.38322170T>C	GRCh38
NC_000015.9:g.38614371T>C , CM000677.1:g.38614371T>C	GRCh37
NC_000015.8:g.36401663T>C	NCBI36
NG_008980.1:g.74320T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.208-71T>C MANE Select	ENSP00000299084.4:n.208-71T>C
ENST00000299084.8:c.208-71T>C	ENSP00000299084.4:n.208-71T>C
ENST00000561205.1:n.546-71T>C
ENST00000561317.1:c.145-71T>C	ENSP00000453680.1:n.145-71T>C
NM_152594.2:c.208-71T>C	NP_689807.1:n.208-71T>C
XM_005254202.2:c.244-71T>C	XP_005254259.1:n.244-71T>C
XM_005254203.3:c.-15-71T>C	XP_005254260.1:n.-15-71T>C
XM_011521288.1:c.145-71T>C	XP_011519590.1:n.145-71T>C
XM_011521289.1:c.145-71T>C	XP_011519591.1:n.145-71T>C
XM_011521290.1:c.145-71T>C	XP_011519592.1:n.145-71T>C
XM_005254202.3:c.244-71T>C	XP_005254259.1:n.244-71T>C
XM_011521289.3:c.145-71T>C	XP_011519591.1:n.145-71T>C
NM_152594.3:c.208-71T>C MANE Select	NP_689807.1:n.208-71T>C