Canonical Allele Identifier: CA1469632619

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476747C= , CM000666.2:g.76476747C=	GRCh38
NC_000004.11:g.77397900C= , CM000666.1:g.77397900C=	GRCh37
NC_000004.10:g.77616924C=	NCBI36
NG_028077.1:g.46648C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40527C= MANE Select	ENSP00000296043.6:n.168+40527C=
ENST00000296043.6:c.168+40527C=	ENSP00000296043.6:n.168+40527C=
ENST00000466541.1:n.75+40527C=
ENST00000497440.5:n.109+40527C=
NM_020859.3:c.168+40527C=	NP_065910.3:n.168+40527C=
XM_005263162.3:c.168+40527C=	XP_005263219.1:n.168+40527C=
XM_011532158.1:c.168+40527C=	XP_011530460.1:n.168+40527C=
XM_011532159.1:c.168+40527C=	XP_011530461.1:n.168+40527C=
XM_011532158.3:c.168+40527C=	XP_011530460.1:n.168+40527C=
NM_020859.4:c.168+40527C= MANE Select	NP_065910.3:n.168+40527C=