Canonical Allele Identifier: CA2021314718

Gene: ABCC9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21844982_21844983delinsCA , CM000674.2:g.21844982_21844983delinsCA	GRCh38
NC_000012.11:g.21997916_21997917delinsCA , CM000674.1:g.21997916_21997917delinsCA	GRCh37
NC_000012.10:g.21889183_21889184delinsCA	NCBI36
NG_012819.1:g.96712_96713delinsTG , LRG_377:g.96712_96713delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261201.10:c.3097-68_3097-67delinsTG	ENSP00000261201.4:n.3097-68_3097-67delinsTG
ENST00000682068.1:c.3097-68_3097-67delinsTG	ENSP00000507226.1:n.3097-68_3097-67delinsTG
ENST00000682426.1:n.674-68_674-67delinsTG
ENST00000682879.1:c.*2195-68_*2195-67delinsTG	ENSP00000508210.1:n.*2195-68_*2195-67delinsTG
ENST00000683105.1:c.3097-68_3097-67delinsTG	ENSP00000506801.1:n.3097-68_3097-67delinsTG
ENST00000683676.1:c.3097-68_3097-67delinsTG	ENSP00000508167.1:n.3097-68_3097-67delinsTG
ENST00000683811.1:n.2598-68_2598-67delinsTG
ENST00000684084.1:c.3046-68_3046-67delinsTG	ENSP00000507859.1:n.3046-68_3046-67delinsTG
ENST00000261200.9:c.3097-68_3097-67delinsTG MANE Select	ENSP00000261200.4:n.3097-68_3097-67delinsTG
ENST00000261201.9:c.3097-68_3097-67delinsTG	ENSP00000261201.4:n.3097-68_3097-67delinsTG
ENST00000261200.8:c.3097-68_3097-67delinsTG	ENSP00000261200.4:n.3097-68_3097-67delinsTG
ENST00000261201.8:c.3097-68_3097-67delinsTG	ENSP00000261201.4:n.3097-68_3097-67delinsTG
ENST00000544039.5:c.1978-68_1978-67delinsTG	ENSP00000440521.1:n.1978-68_1978-67delinsTG
NM_005691.3:c.3097-68_3097-67delinsTG	NP_005682.2:n.3097-68_3097-67delinsTG
NM_020297.3:c.3097-68_3097-67delinsTG	NP_064693.2:n.3097-68_3097-67delinsTG
XM_005253284.2:c.3097-68_3097-67delinsTG	XP_005253341.1:n.3097-68_3097-67delinsTG
XM_005253286.2:c.3097-68_3097-67delinsTG	XP_005253343.1:n.3097-68_3097-67delinsTG
XM_005253287.3:c.3097-68_3097-67delinsTG	XP_005253344.1:n.3097-68_3097-67delinsTG
XM_005253288.2:c.3097-68_3097-67delinsTG	XP_005253345.1:n.3097-68_3097-67delinsTG
XM_005253289.2:c.3058-68_3058-67delinsTG	XP_005253346.1:n.3058-68_3058-67delinsTG
XM_005253290.2:c.2956-68_2956-67delinsTG	XP_005253347.1:n.2956-68_2956-67delinsTG
XM_006719025.2:c.3058-68_3058-67delinsTG	XP_006719088.1:n.3058-68_3058-67delinsTG
XM_011520545.1:c.3097-68_3097-67delinsTG	XP_011518847.1:n.3097-68_3097-67delinsTG
XM_005253284.4:c.3097-68_3097-67delinsTG	XP_005253341.1:n.3097-68_3097-67delinsTG
XM_005253286.4:c.3097-68_3097-67delinsTG	XP_005253343.1:n.3097-68_3097-67delinsTG
XM_005253287.5:c.3097-68_3097-67delinsTG	XP_005253344.1:n.3097-68_3097-67delinsTG
XM_005253288.4:c.3097-68_3097-67delinsTG	XP_005253345.1:n.3097-68_3097-67delinsTG
XM_005253289.4:c.3058-68_3058-67delinsTG	XP_005253346.1:n.3058-68_3058-67delinsTG
XM_005253290.4:c.2956-68_2956-67delinsTG	XP_005253347.1:n.2956-68_2956-67delinsTG
XM_006719025.4:c.3058-68_3058-67delinsTG	XP_006719088.1:n.3058-68_3058-67delinsTG
XM_011520545.3:c.3097-68_3097-67delinsTG	XP_011518847.1:n.3097-68_3097-67delinsTG
NM_001377273.1:c.3097-68_3097-67delinsTG	NP_001364202.1:n.3097-68_3097-67delinsTG
NM_001377274.1:c.2230-68_2230-67delinsTG	NP_001364203.1:n.2230-68_2230-67delinsTG
NM_005691.4:c.3097-68_3097-67delinsTG	NP_005682.2:n.3097-68_3097-67delinsTG
NM_020297.4:c.3097-68_3097-67delinsTG MANE Select	NP_064693.2:n.3097-68_3097-67delinsTG