Canonical Allele Identifier: CA11824533

Gene: AFAP1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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