Canonical Allele Identifier: CA391931934

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38614467A>C (hg19) ; chr15:g.38322266A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322266A>C , CM000677.2:g.38322266A>C	GRCh38
NC_000015.9:g.38614467A>C , CM000677.1:g.38614467A>C	GRCh37
NC_000015.8:g.36401759A>C	NCBI36
NG_008980.1:g.74416A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.233A>C MANE Select	ENSP00000299084.4:p.Lys78Thr
ENST00000299084.8:c.233A>C	ENSP00000299084.4:p.Lys78Thr
ENST00000561205.1:n.571A>C
ENST00000561317.1:c.170A>C	ENSP00000453680.1:p.Lys57Thr
NM_152594.2:c.233A>C	NP_689807.1:p.Lys78Thr
XM_005254202.2:c.269A>C	XP_005254259.1:p.Lys90Thr
XM_005254203.3:c.11A>C	XP_005254260.1:p.Lys4Thr
XM_011521288.1:c.170A>C	XP_011519590.1:p.Lys57Thr
XM_011521289.1:c.170A>C	XP_011519591.1:p.Lys57Thr
XM_011521290.1:c.170A>C	XP_011519592.1:p.Lys57Thr
XM_005254202.3:c.269A>C	XP_005254259.1:p.Lys90Thr
XM_011521289.3:c.170A>C	XP_011519591.1:p.Lys57Thr
NM_152594.3:c.233A>C MANE Select	NP_689807.1:p.Lys78Thr