Canonical Allele Identifier: CA2575673329
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351731A>G , CM000677.2:g.38351731A>G GRCh38
NC_000015.9:g.38643932A>G , CM000677.1:g.38643932A>G GRCh37
NC_000015.8:g.36431224A>G NCBI36
NG_008980.1:g.103881A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.*67A>G MANE Select ENSP00000299084.4:n.*67A>G
ENST00000299084.8:c.*67A>G ENSP00000299084.4:n.*67A>G
NM_152594.2:c.*67A>G NP_689807.1:n.*67A>G
XM_005254202.2:c.*67A>G XP_005254259.1:n.*67A>G
XM_005254203.3:c.*67A>G XP_005254260.1:n.*67A>G
XM_011521288.1:c.*67A>G XP_011519590.1:n.*67A>G
XM_011521289.1:c.*67A>G XP_011519591.1:n.*67A>G
XM_011521290.1:c.*67A>G XP_011519592.1:n.*67A>G
XM_005254202.3:c.*67A>G XP_005254259.1:n.*67A>G
XM_011521289.3:c.*67A>G XP_011519591.1:n.*67A>G
NM_152594.3:c.*67A>G MANE Select NP_689807.1:n.*67A>G