Canonical Allele Identifier: CA1436651846
Gene: AFAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.7938188G>A , CM000666.2:g.7938188G>A GRCh38
NC_000004.11:g.7939915G>A , CM000666.1:g.7939915G>A GRCh37
NC_000004.10:g.7990815G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000420658.6:c.-3+1468C>T MANE Select ENSP00000410689.1:n.-3+1468C>T
ENST00000358461.6:c.-3+1468C>T ENSP00000351245.2:n.-3+1468C>T
ENST00000420658.5:c.-3+1468C>T ENSP00000410689.1:n.-3+1468C>T
NM_001134647.1:c.-3+1468C>T NP_001128119.1:n.-3+1468C>T
NM_198595.2:c.-3+1468C>T NP_940997.1:n.-3+1468C>T
XM_006713908.2:c.61+404C>T XP_006713971.1:n.61+404C>T
XM_006713909.2:c.61+404C>T XP_006713972.1:n.61+404C>T
XM_011513545.1:c.61+404C>T XP_011511847.1:n.61+404C>T
XM_011513546.1:c.61+404C>T XP_011511848.1:n.61+404C>T
XM_006713909.3:c.61+404C>T XP_006713972.1:n.61+404C>T
NM_001371091.1:c.-781+1468C>T NP_001358020.1:n.-781+1468C>T
NM_001134647.2:c.-3+1468C>T MANE Select NP_001128119.1:n.-3+1468C>T
NM_198595.3:c.-3+1468C>T NP_940997.1:n.-3+1468C>T