Canonical Allele Identifier: CA2197068397

Gene: MCTP2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.94396279G>C , CM000677.2:g.94396279G>C	GRCh38
NC_000015.9:g.94939508G>C , CM000677.1:g.94939508G>C	GRCh37
NC_000015.8:g.92740512G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357742.10:c.1789-2682G>C MANE Select	ENSP00000350377.4:n.1789-2682G>C
ENST00000357742.9:c.1789-2682G>C	ENSP00000350377.4:n.1789-2682G>C
ENST00000357742.8:c.1789-2682G>C	ENSP00000350377.4:n.1789-2682G>C
ENST00000451018.7:c.1789-2682G>C	ENSP00000395109.3:n.1789-2682G>C
ENST00000456504.5:c.*1327-2682G>C	ENSP00000388887.1:n.*1327-2682G>C
ENST00000557742.1:c.553-2682G>C	ENSP00000454847.1:n.553-2682G>C
NM_001159643.1:c.1789-2682G>C	NP_001153115.1:n.1789-2682G>C
NM_001159644.1:c.553-2682G>C	NP_001153116.1:n.553-2682G>C
NM_018349.3:c.1789-2682G>C	NP_060819.3:n.1789-2682G>C
XM_005254955.2:c.1789-2682G>C	XP_005255012.1:n.1789-2682G>C
XM_005254960.1:c.553-2682G>C	XP_005255017.1:n.553-2682G>C
XM_006720603.2:c.1789-2682G>C	XP_006720666.1:n.1789-2682G>C
XM_011521770.1:c.1789-2682G>C	XP_011520072.1:n.1789-2682G>C
XM_011521771.1:c.1789-2682G>C	XP_011520073.1:n.1789-2682G>C
XM_011521772.1:c.1789-2682G>C	XP_011520074.1:n.1789-2682G>C
XM_011521773.1:c.1789-2682G>C	XP_011520075.1:n.1789-2682G>C
XM_011521774.1:c.1789-2682G>C	XP_011520076.1:n.1789-2682G>C
XM_011521775.1:c.673-2682G>C	XP_011520077.1:n.673-2682G>C
XR_931865.1:n.1854-2682G>C
XM_005254955.4:c.1789-2682G>C	XP_005255012.1:n.1789-2682G>C
XM_005254960.2:c.553-2682G>C	XP_005255017.1:n.553-2682G>C
XM_011521771.2:c.1789-2682G>C	XP_011520073.1:n.1789-2682G>C
XM_011521772.2:c.1789-2682G>C	XP_011520074.1:n.1789-2682G>C
XM_011521773.2:c.1789-2682G>C	XP_011520075.1:n.1789-2682G>C
XM_011521774.2:c.1789-2682G>C	XP_011520076.1:n.1789-2682G>C
XM_011521775.2:c.673-2682G>C	XP_011520077.1:n.673-2682G>C
XM_017022403.1:c.1753-2682G>C	XP_016877892.1:n.1753-2682G>C
XM_017022404.1:c.1789-2682G>C	XP_016877893.1:n.1789-2682G>C
XM_017022405.1:c.1789-2682G>C	XP_016877894.1:n.1789-2682G>C
XM_024449982.1:c.1507-2682G>C	XP_024305750.1:n.1507-2682G>C
XR_931865.2:n.1854-2682G>C
NM_001159644.2:c.553-2682G>C	NP_001153116.1:n.553-2682G>C
NM_001159643.2:c.1789-2682G>C	NP_001153115.1:n.1789-2682G>C
NM_001385001.1:c.1789-2682G>C MANE Select	NP_001371930.1:n.1789-2682G>C
NM_001385002.1:c.1789-2682G>C	NP_001371931.1:n.1789-2682G>C
NM_001385003.1:c.1789-2682G>C	NP_001371932.1:n.1789-2682G>C
NM_001385004.1:c.1789-2682G>C	NP_001371933.1:n.1789-2682G>C
NM_001385005.1:c.1789-2682G>C	NP_001371934.1:n.1789-2682G>C
NM_001385006.1:c.1789-2682G>C	NP_001371935.1:n.1789-2682G>C
NM_001385007.1:c.1507-2682G>C	NP_001371936.1:n.1507-2682G>C
NM_001385008.1:c.1789-2682G>C	NP_001371937.1:n.1789-2682G>C
NM_001385009.1:c.1291-2682G>C	NP_001371938.1:n.1291-2682G>C
NM_001385010.1:c.1291-2682G>C	NP_001371939.1:n.1291-2682G>C
NM_001385011.1:c.1471-2682G>C	NP_001371940.1:n.1471-2682G>C
NM_018349.4:c.1789-2682G>C	NP_060819.3:n.1789-2682G>C
NR_169526.1:n.1893-2682G>C
NR_169527.1:n.2296-2682G>C
NR_169528.1:n.2096-2682G>C
NR_169529.1:n.2361-2682G>C
NR_169530.1:n.2334-2682G>C
NR_169531.1:n.1958-2682G>C
NR_169532.1:n.2437-2682G>C