Canonical Allele Identifier: CA493799116

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16163187-C-T
• MyVariant Identifiers: chr16:g.16257044C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163187C>T , CM000678.2:g.16163187C>T	GRCh38
NC_000016.9:g.16257044C>T , CM000678.1:g.16257044C>T	GRCh37
NC_000016.8:g.16164545C>T	NCBI36
NG_007558.2:g.65285G>A
NG_007558.3:g.65431G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3312G>A	ENSP00000483331.2:p.Leu1104=
ENST00000205557.12:c.3312G>A MANE Select	ENSP00000205557.7:p.Leu1104=
ENST00000640696.1:c.321-1623G>A	ENSP00000492197.1:n.321-1623G>A
ENST00000205557.11:c.3312G>A	ENSP00000205557.7:p.Leu1104=
ENST00000456970.6:c.3132-1623G>A	ENSP00000405002.2:n.3132-1623G>A
ENST00000622290.4:c.*521G>A	ENSP00000483331.1:n.*521G>A
NM_001171.5:c.3312G>A	NP_001162.4:p.Leu1104=
XM_011522479.1:c.3279G>A	XP_011520781.1:p.Leu1093=
XM_011522480.1:c.2970G>A	XP_011520782.1:p.Leu990=
XM_011522481.1:c.2970G>A	XP_011520783.1:p.Leu990=
XR_932836.1:n.3547G>A
XR_932837.1:n.3543-1623G>A
XR_932838.1:n.3543-1623G>A
XR_933133.1:n.407+344C>T
XR_933134.1:n.754+344C>T
NM_001351800.1:c.2970G>A	NP_001338729.1:p.Leu990=
NR_147784.1:n.3169-1623G>A
XM_011522479.2:c.3279G>A	XP_011520781.1:p.Leu1093=
XM_011522481.3:c.2970G>A	XP_011520783.1:p.Leu990=
XM_017023212.1:c.3144G>A	XP_016878701.1:p.Leu1048=
XM_017023214.1:c.3307-1623G>A	XP_016878703.1:n.3307-1623G>A
XM_024450261.1:c.3348G>A	XP_024306029.1:p.Leu1116=
XR_932836.2:n.3493G>A
XR_932837.3:n.3488-1623G>A
XR_932838.3:n.3488-1623G>A
NM_001171.6:c.3312G>A MANE Select	NP_001162.5:p.Leu1104=