Canonical Allele Identifier: CA1425384266

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183042126_183042127delinsTA , CM000665.2:g.183042126_183042127delinsTA	GRCh38
NC_000003.11:g.182759914_182759915delinsTA , CM000665.1:g.182759914_182759915delinsTA	GRCh37
NC_000003.10:g.184242608_184242609delinsTA	NCBI36
NG_008100.1:g.62451_62452delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000265594.9:c.1084-377_1084-376delinsTA MANE Select	ENSP00000265594.4:n.1084-377_1084-376delinsTA
ENST00000265594.8:c.1084-377_1084-376delinsTA	ENSP00000265594.4:n.1084-377_1084-376delinsTA
ENST00000476176.5:c.943-377_943-376delinsTA	ENSP00000420433.1:n.943-377_943-376delinsTA
ENST00000492597.5:c.757-377_757-376delinsTA	ENSP00000419898.1:n.757-377_757-376delinsTA
ENST00000495767.5:c.*665-377_*665-376delinsTA	ENSP00000419658.1:n.*665-377_*665-376delinsTA
ENST00000497830.5:c.*681-377_*681-376delinsTA	ENSP00000420088.1:n.*681-377_*681-376delinsTA
ENST00000497959.5:c.970-377_970-376delinsTA	ENSP00000420648.1:n.970-377_970-376delinsTA
ENST00000539926.5:c.634-377_634-376delinsTA	ENSP00000441253.2:n.634-377_634-376delinsTA
ENST00000610757.4:c.634-377_634-376delinsTA	ENSP00000480435.1:n.634-377_634-376delinsTA
ENST00000629669.2:c.970-377_970-376delinsTA	ENSP00000486824.1:n.970-377_970-376delinsTA
NM_001293273.1:c.733-377_733-376delinsTA	NP_001280202.1:n.733-377_733-376delinsTA
NM_020166.4:c.1084-377_1084-376delinsTA	NP_064551.3:n.1084-377_1084-376delinsTA
NR_120639.1:n.998-377_998-376delinsTA
NR_120640.1:n.1751-377_1751-376delinsTA
XM_006713702.1:c.757-377_757-376delinsTA	XP_006713765.1:n.757-377_757-376delinsTA
XM_011512992.1:c.970-377_970-376delinsTA	XP_011511294.1:n.970-377_970-376delinsTA
XM_011512993.1:c.1084-377_1084-376delinsTA	XP_011511295.1:n.1084-377_1084-376delinsTA
XR_241502.2:n.1231-377_1231-376delinsTA
XR_924159.1:n.1231-377_1231-376delinsTA
NM_001363880.1:c.757-377_757-376delinsTA	NP_001350809.1:n.757-377_757-376delinsTA
XM_011512992.2:c.970-377_970-376delinsTA	XP_011511294.1:n.970-377_970-376delinsTA
XR_001740207.2:n.1207-377_1207-376delinsTA
XR_001740208.2:n.1207-377_1207-376delinsTA
XR_001740209.2:n.1177-377_1177-376delinsTA
XR_001740210.1:n.1037-377_1037-376delinsTA
XR_002959553.1:n.1207-377_1207-376delinsTA
XR_002959554.1:n.1207-377_1207-376delinsTA
XR_241502.3:n.1177-377_1177-376delinsTA
NM_020166.5:c.1084-377_1084-376delinsTA MANE Select	NP_064551.3:n.1084-377_1084-376delinsTA
NM_001293273.2:c.733-377_733-376delinsTA	NP_001280202.1:n.733-377_733-376delinsTA
NR_120639.2:n.907-377_907-376delinsTA
NR_120640.2:n.1751-377_1751-376delinsTA