Canonical Allele Identifier: CA1425384352

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183042340A= , CM000665.2:g.183042340A=	GRCh38
NC_000003.11:g.182760128A= , CM000665.1:g.182760128A=	GRCh37
NC_000003.10:g.184242822A=	NCBI36
NG_008100.1:g.62238T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265594.9:c.1084-590T= MANE Select	ENSP00000265594.4:n.1084-590T=
ENST00000265594.8:c.1084-590T=	ENSP00000265594.4:n.1084-590T=
ENST00000476176.5:c.943-590T=	ENSP00000420433.1:n.943-590T=
ENST00000492597.5:c.757-590T=	ENSP00000419898.1:n.757-590T=
ENST00000495767.5:c.*665-590T=	ENSP00000419658.1:n.*665-590T=
ENST00000497830.5:c.*681-590T=	ENSP00000420088.1:n.*681-590T=
ENST00000497959.5:c.970-590T=	ENSP00000420648.1:n.970-590T=
ENST00000539926.5:c.634-590T=	ENSP00000441253.2:n.634-590T=
ENST00000610757.4:c.634-590T=	ENSP00000480435.1:n.634-590T=
ENST00000629669.2:c.970-590T=	ENSP00000486824.1:n.970-590T=
NM_001293273.1:c.733-590T=	NP_001280202.1:n.733-590T=
NM_020166.4:c.1084-590T=	NP_064551.3:n.1084-590T=
NR_120639.1:n.998-590T=
NR_120640.1:n.1751-590T=
XM_006713702.1:c.757-590T=	XP_006713765.1:n.757-590T=
XM_011512992.1:c.970-590T=	XP_011511294.1:n.970-590T=
XM_011512993.1:c.1084-590T=	XP_011511295.1:n.1084-590T=
XR_241502.2:n.1231-590T=
XR_924159.1:n.1231-590T=
NM_001363880.1:c.757-590T=	NP_001350809.1:n.757-590T=
XM_011512992.2:c.970-590T=	XP_011511294.1:n.970-590T=
XR_001740207.2:n.1207-590T=
XR_001740208.2:n.1207-590T=
XR_001740209.2:n.1177-590T=
XR_001740210.1:n.1037-590T=
XR_002959553.1:n.1207-590T=
XR_002959554.1:n.1207-590T=
XR_241502.3:n.1177-590T=
NM_020166.5:c.1084-590T= MANE Select	NP_064551.3:n.1084-590T=
NM_001293273.2:c.733-590T=	NP_001280202.1:n.733-590T=
NR_120639.2:n.907-590T=
NR_120640.2:n.1751-590T=