Canonical Allele Identifier: CA1573632564

Gene: MCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064136C= , CM000667.2:g.113064136C=	GRCh38
NC_000005.9:g.112399833C= , CM000667.1:g.112399833C=	GRCh37
NC_000005.8:g.112427732C=	NCBI36
NG_012265.1:g.429695G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1491G=	ENSP00000305617.4:p.Gln497=
ENST00000408903.7:c.2061G= MANE Select	ENSP00000386227.3:p.Gln687=
ENST00000302475.8:c.1491G=	ENSP00000305617.4:p.Gln497=
ENST00000408903.6:c.2061G=	ENSP00000386227.3:p.Gln687=
ENST00000514701.5:c.1491G=	ENSP00000485220.1:p.Gln497=
ENST00000515367.6:c.1302G=	ENSP00000421615.2:p.Gln434=
NM_001085377.1:c.2061G=	NP_001078846.1:p.Gln687=
NM_002387.2:c.1491G=	NP_002378.1:p.Gln497=
XM_005271991.2:c.1491G=	XP_005272048.1:p.Gln497=
XM_005271991.3:c.1491G=	XP_005272048.1:p.Gln497=
XM_017009473.1:c.2061G=	XP_016864962.1:p.Gln687=
XM_017009474.1:c.1461G=	XP_016864963.1:p.Gln487=
XM_024446049.1:c.1302G=	XP_024301817.1:p.Gln434=
XM_024446050.1:c.1302G=	XP_024301818.1:p.Gln434=
XM_024446051.1:c.1302G=	XP_024301819.1:p.Gln434=
XM_024446052.1:c.1302G=	XP_024301820.1:p.Gln434=
NM_001085377.2:c.2061G= MANE Select	NP_001078846.2:p.Gln687=
NM_002387.3:c.1491G=	NP_002378.2:p.Gln497=