Canonical Allele Identifier: CA394885057

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263694T>A (hg19) ; chr16:g.16169837T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169837T>A , CM000678.2:g.16169837T>A	GRCh38
NC_000016.9:g.16263694T>A , CM000678.1:g.16263694T>A	GRCh37
NC_000016.8:g.16171195T>A	NCBI36
NG_007558.2:g.58635A>T
NG_007558.3:g.58781A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2804A>T	ENSP00000483331.2:p.His935Leu
ENST00000205557.12:c.2804A>T MANE Select	ENSP00000205557.7:p.His935Leu
ENST00000205557.11:c.2804A>T	ENSP00000205557.7:p.His935Leu
ENST00000456970.6:c.2629A>T	ENSP00000405002.2:n.2629A>T
ENST00000622290.4:c.*13A>T	ENSP00000483331.1:n.*13A>T
NM_001171.5:c.2804A>T	NP_001162.4:p.His935Leu
XM_011522479.1:c.2771A>T	XP_011520781.1:p.His924Leu
XM_011522480.1:c.2462A>T	XP_011520782.1:p.His821Leu
XM_011522481.1:c.2462A>T	XP_011520783.1:p.His821Leu
XR_932836.1:n.3039A>T
XR_932837.1:n.3040A>T
XR_932838.1:n.3040A>T
NM_001351800.1:c.2462A>T	NP_001338729.1:p.His821Leu
NR_147784.1:n.2666A>T
XM_011522479.2:c.2771A>T	XP_011520781.1:p.His924Leu
XM_011522481.3:c.2462A>T	XP_011520783.1:p.His821Leu
XM_017023212.1:c.2636A>T	XP_016878701.1:p.His879Leu
XM_017023214.1:c.2804A>T	XP_016878703.1:p.His935Leu
XM_024450261.1:c.2840A>T	XP_024306029.1:p.His947Leu
XR_932836.2:n.2985A>T
XR_932837.3:n.2985A>T
XR_932838.3:n.2985A>T
NM_001171.6:c.2804A>T MANE Select	NP_001162.5:p.His935Leu