Canonical Allele Identifier: CA1931489559

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830555_99830559delinsGTTTC , CM000672.2:g.99830555_99830559delinsGTTTC	GRCh38
NC_000010.10:g.101590312_101590316delinsGTTTC , CM000672.1:g.101590312_101590316delinsGTTTC	GRCh37
NC_000010.9:g.101580302_101580306delinsGTTTC	NCBI36
NG_011798.1:g.52850_52854delinsGTTTC
NG_011798.2:g.52958_52962delinsGTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+122_2747+126delinsGTTTC MANE Select	ENSP00000497274.1:n.2747+122_2747+126delinsGTTTC
ENST00000370449.8:c.2747+122_2747+126delinsGTTTC	ENSP00000359478.4:n.2747+122_2747+126delinsGTTTC
NM_000392.4:c.2747+122_2747+126delinsGTTTC	NP_000383.1:n.2747+122_2747+126delinsGTTTC
XM_006717630.2:c.2051+122_2051+126delinsGTTTC	XP_006717693.1:n.2051+122_2051+126delinsGTTTC
XM_011539291.1:c.2747+122_2747+126delinsGTTTC	XP_011537593.1:n.2747+122_2747+126delinsGTTTC
XR_945604.1:n.2936+122_2936+126delinsGTTTC
XR_945605.1:n.2938+122_2938+126delinsGTTTC
NM_000392.5:c.2747+122_2747+126delinsGTTTC MANE Select	NP_000383.2:n.2747+122_2747+126delinsGTTTC
XM_006717630.3:c.2051+122_2051+126delinsGTTTC	XP_006717693.1:n.2051+122_2051+126delinsGTTTC
XM_011539291.3:c.2747+122_2747+126delinsGTTTC	XP_011537593.1:n.2747+122_2747+126delinsGTTTC
XR_945604.3:n.2990+122_2990+126delinsGTTTC
XR_945605.3:n.2990+122_2990+126delinsGTTTC