Canonical Allele Identifier: CA2112209624
Gene: ABCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95122995_95122997delinsCAT , CM000675.2:g.95122995_95122997delinsCAT GRCh38
NC_000013.10:g.95775249_95775251delinsCAT , CM000675.1:g.95775249_95775251delinsCAT GRCh37
NC_000013.9:g.94573250_94573252delinsCAT NCBI36
NG_050651.1:g.183450_183452delinsATG
NG_050651.2:g.183450_183452delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000643051.1:c.*81-6996_*81-6994delinsATG ENSP00000495513.1:n.*81-6996_*81-6994delinsATG
ENST00000643556.1:c.2597-6996_2597-6994delinsATG ENSP00000494938.1:n.2597-6996_2597-6994delinsATG
ENST00000643816.1:n.2739-6996_2739-6994delinsATG
ENST00000643842.1:c.*2502-6996_*2502-6994delinsATG ENSP00000493861.1:n.*2502-6996_*2502-6994delinsATG
ENST00000644880.1:n.66-6996_66-6994delinsATG
ENST00000645237.2:c.2456-6996_2456-6994delinsATG MANE Select ENSP00000494609.1:n.2456-6996_2456-6994delinsATG
ENST00000646439.1:c.2315-6996_2315-6994delinsATG ENSP00000494751.1:n.2315-6996_2315-6994delinsATG
ENST00000376887.8:c.2456-6996_2456-6994delinsATG ENSP00000366084.4:n.2456-6996_2456-6994delinsATG
ENST00000536256.3:c.2231-6996_2231-6994delinsATG ENSP00000442024.1:n.2231-6996_2231-6994delinsATG
ENST00000629385.1:c.2456-6996_2456-6994delinsATG ENSP00000487081.1:n.2456-6996_2456-6994delinsATG
NM_001105515.2:c.2456-6996_2456-6994delinsATG NP_001098985.1:n.2456-6996_2456-6994delinsATG
NM_001301829.1:c.2315-6996_2315-6994delinsATG NP_001288758.1:n.2315-6996_2315-6994delinsATG
NM_001301830.1:c.2231-6996_2231-6994delinsATG NP_001288759.1:n.2231-6996_2231-6994delinsATG
NM_005845.4:c.2456-6996_2456-6994delinsATG NP_005836.2:n.2456-6996_2456-6994delinsATG
XM_005254025.2:c.2327-6996_2327-6994delinsATG XP_005254082.1:n.2327-6996_2327-6994delinsATG
XM_006719914.1:c.2366-6996_2366-6994delinsATG XP_006719977.1:n.2366-6996_2366-6994delinsATG
XM_011521047.1:c.1907-6996_1907-6994delinsATG XP_011519349.1:n.1907-6996_1907-6994delinsATG
XM_017020319.1:c.2327-6996_2327-6994delinsATG XP_016875808.1:n.2327-6996_2327-6994delinsATG
XM_017020321.1:c.941-6996_941-6994delinsATG XP_016875810.1:n.941-6996_941-6994delinsATG
XM_017020322.1:c.2327-6996_2327-6994delinsATG XP_016875811.1:n.2327-6996_2327-6994delinsATG
NM_001105515.3:c.2456-6996_2456-6994delinsATG NP_001098985.1:n.2456-6996_2456-6994delinsATG
NM_001301829.2:c.2315-6996_2315-6994delinsATG NP_001288758.1:n.2315-6996_2315-6994delinsATG
NM_001301830.2:c.2231-6996_2231-6994delinsATG NP_001288759.1:n.2231-6996_2231-6994delinsATG
NM_005845.5:c.2456-6996_2456-6994delinsATG MANE Select NP_005836.2:n.2456-6996_2456-6994delinsATG