Canonical Allele Identifier: CA1469632863

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476961C= , CM000666.2:g.76476961C=	GRCh38
NC_000004.11:g.77398114C= , CM000666.1:g.77398114C=	GRCh37
NC_000004.10:g.77617138C=	NCBI36
NG_028077.1:g.46862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40741C= MANE Select	ENSP00000296043.6:n.168+40741C=
ENST00000296043.6:c.168+40741C=	ENSP00000296043.6:n.168+40741C=
ENST00000466541.1:n.75+40741C=
ENST00000497440.5:n.109+40741C=
NM_020859.3:c.168+40741C=	NP_065910.3:n.168+40741C=
XM_005263162.3:c.168+40741C=	XP_005263219.1:n.168+40741C=
XM_011532158.1:c.168+40741C=	XP_011530460.1:n.168+40741C=
XM_011532159.1:c.168+40741C=	XP_011530461.1:n.168+40741C=
XM_011532158.3:c.168+40741C=	XP_011530460.1:n.168+40741C=
NM_020859.4:c.168+40741C= MANE Select	NP_065910.3:n.168+40741C=