Canonical Allele Identifier: CA2631959779

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16155230-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155231dup , CM000678.2:g.16155231dup	GRCh38
NC_000016.9:g.16249088dup , CM000678.1:g.16249088dup	GRCh37
NC_000016.8:g.16156589dup	NCBI36
NG_007558.2:g.73241dup
NG_007558.3:g.73387dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.546dup
ENST00000622290.5:c.*55-200dup	ENSP00000483331.2:n.*55-200dup
ENST00000205557.12:c.3883-200dup MANE Select	ENSP00000205557.7:n.3883-200dup
ENST00000640696.1:c.697-200dup	ENSP00000492197.1:n.697-200dup
ENST00000205557.11:c.3883-200dup	ENSP00000205557.7:n.3883-200dup
ENST00000456970.6:c.3508-200dup	ENSP00000405002.2:n.3508-200dup
ENST00000576204.5:n.546dup
ENST00000622290.4:c.*1092-200dup	ENSP00000483331.1:n.*1092-200dup
NM_001171.5:c.3883-200dup	NP_001162.4:n.3883-200dup
XM_011522479.1:c.3850-200dup	XP_011520781.1:n.3850-200dup
XM_011522480.1:c.3541-200dup	XP_011520782.1:n.3541-200dup
XM_011522481.1:c.3541-200dup	XP_011520783.1:n.3541-200dup
XR_932836.1:n.4181-200dup
XR_932837.1:n.3919-200dup
XR_932838.1:n.3982-200dup
XR_933134.1:n.539-4550dup
NM_001351800.1:c.3541-200dup	NP_001338729.1:n.3541-200dup
NR_147784.1:n.3545-200dup
XM_011522479.2:c.3850-200dup	XP_011520781.1:n.3850-200dup
XM_011522481.3:c.3541-200dup	XP_011520783.1:n.3541-200dup
XM_017023212.1:c.3715-200dup	XP_016878701.1:n.3715-200dup
XM_024450261.1:c.3919-200dup	XP_024306029.1:n.3919-200dup
XR_932836.2:n.4127-200dup
XR_932837.3:n.3864-200dup
XR_932838.3:n.3927-200dup
NM_001171.6:c.3883-200dup MANE Select	NP_001162.5:n.3883-200dup