Canonical Allele Identifier: CA1436651845

Gene: AFAP1

Genomic Alleles

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

Transcript Alleles

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