Canonical Allele Identifier: CA1373064942

Gene: FRMD4B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69178228A= , CM000665.2:g.69178228A=	GRCh38
NC_000003.11:g.69227379A= , CM000665.1:g.69227379A=	GRCh37
NC_000003.10:g.69310069A=	NCBI36
NG_034059.1:g.213077T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398540.8:c.2852-1572T= MANE Select	ENSP00000381549.3:n.2852-1572T=
ENST00000398540.7:c.2852-1572T=	ENSP00000381549.3:n.2852-1572T=
ENST00000478263.5:c.1808-1572T=	ENSP00000418682.1:n.1808-1572T=
NM_015123.2:c.2852-1572T=	NP_055938.1:n.2852-1572T=
XM_005264721.2:c.2885-1572T=	XP_005264778.2:n.2885-1572T=
XM_005264722.1:c.2717-1572T=	XP_005264779.1:n.2717-1572T=
XM_005264723.1:c.1808-1572T=	XP_005264780.1:n.1808-1572T=
XM_006713063.2:c.2690-1572T=	XP_006713126.1:n.2690-1572T=
XM_006713064.1:c.1985-1572T=	XP_006713127.1:n.1985-1572T=
XM_011533526.1:c.2690-1572T=	XP_011531828.1:n.2690-1572T=
XM_011533527.1:c.2117-1572T=	XP_011531829.1:n.2117-1572T=
XM_017005989.1:c.2852-1572T=	XP_016861478.1:n.2852-1572T=
XM_017005990.1:c.2717-1572T=	XP_016861479.1:n.2717-1572T=
XM_017005991.1:c.2690-1572T=	XP_016861480.1:n.2690-1572T=
XM_017005992.1:c.2690-1572T=	XP_016861481.1:n.2690-1572T=
XM_017005993.1:c.2690-1572T=	XP_016861482.1:n.2690-1572T=
XM_017005994.1:c.2690-1572T=	XP_016861483.1:n.2690-1572T=
XM_017005995.1:c.2117-1572T=	XP_016861484.1:n.2117-1572T=
XM_017005996.1:c.1985-1572T=	XP_016861485.1:n.1985-1572T=
XM_017005997.1:c.1808-1572T=	XP_016861486.1:n.1808-1572T=
NM_015123.3:c.2852-1572T= MANE Select	NP_055938.2:n.2852-1572T=