Canonical Allele Identifier: CA1931489224

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830401_99830414delinsAGAGAACAGCTTTC , CM000672.2:g.99830401_99830414delinsAGAGAACAGCTTTC	GRCh38
NC_000010.10:g.101590158_101590171delinsAGAGAACAGCTTTC , CM000672.1:g.101590158_101590171delinsAGAGAACAGCTTTC	GRCh37
NC_000010.9:g.101580148_101580161delinsAGAGAACAGCTTTC	NCBI36
NG_011798.1:g.52696_52709delinsAGAGAACAGCTTTC
NG_011798.2:g.52804_52817delinsAGAGAACAGCTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2715_2728delinsAGAGAACAGCTTTC MANE Select	ENSP00000497274.1:p.Arg905=
ENST00000370449.8:c.2715_2728delinsAGAGAACAGCTTTC	ENSP00000359478.4:p.Arg905=
NM_000392.4:c.2715_2728delinsAGAGAACAGCTTTC	NP_000383.1:p.Arg905=
XM_006717630.2:c.2019_2032delinsAGAGAACAGCTTTC	XP_006717693.1:p.Arg673=
XM_011539291.1:c.2715_2728delinsAGAGAACAGCTTTC	XP_011537593.1:p.Arg905=
XR_945604.1:n.2904_2917delinsAGAGAACAGCTTTC
XR_945605.1:n.2906_2919delinsAGAGAACAGCTTTC
NM_000392.5:c.2715_2728delinsAGAGAACAGCTTTC MANE Select	NP_000383.2:p.Arg905=
XM_006717630.3:c.2019_2032delinsAGAGAACAGCTTTC	XP_006717693.1:p.Arg673=
XM_011539291.3:c.2715_2728delinsAGAGAACAGCTTTC	XP_011537593.1:p.Arg905=
XR_945604.3:n.2958_2971delinsAGAGAACAGCTTTC
XR_945605.3:n.2958_2971delinsAGAGAACAGCTTTC