Canonical Allele Identifier: CA14130323
Community Standard Title: NM_152594.3(SPRED1):c.685-184C>T
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38350830C>T , CM000677.2:g.38350830C>T GRCh38
NC_000015.9:g.38643031C>T , CM000677.1:g.38643031C>T GRCh37
NC_000015.8:g.36430323C>T NCBI36
NG_008980.1:g.102980C>T

Transcript Alleles

HGVS Amino-acid Change
NM_152594.3:c.685-184C>T MANE Select NP_689807.1:n.685-184C>T
ENST00000299084.9:c.685-184C>T MANE Select ENSP00000299084.4:n.685-184C>T
NM_152594.2:c.685-184C>T NP_689807.1:n.685-184C>T
ENST00000299084.8:c.685-184C>T ENSP00000299084.4:n.685-184C>T
XM_005254202.2:c.721-184C>T XP_005254259.1:n.721-184C>T
XM_005254202.3:c.721-184C>T XP_005254259.1:n.721-184C>T
XM_005254203.3:c.463-184C>T XP_005254260.1:n.463-184C>T
XM_011521288.1:c.622-184C>T XP_011519590.1:n.622-184C>T
XM_011521289.1:c.622-184C>T XP_011519591.1:n.622-184C>T
XM_011521289.3:c.622-184C>T XP_011519591.1:n.622-184C>T
XM_011521290.1:c.622-184C>T XP_011519592.1:n.622-184C>T