Canonical Allele Identifier: CA494088374

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16259588C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165731C>G , CM000678.2:g.16165731C>G	GRCh38
NC_000016.9:g.16259588C>G , CM000678.1:g.16259588C>G	GRCh37
NC_000016.8:g.16167089C>G	NCBI36
NG_007558.2:g.62741G>C
NG_007558.3:g.62887G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3198G>C	ENSP00000483331.2:p.Leu1066=
ENST00000205557.12:c.3198G>C MANE Select	ENSP00000205557.7:p.Leu1066=
ENST00000640696.1:c.213G>C	ENSP00000492197.1:p.Leu71=
ENST00000205557.11:c.3198G>C	ENSP00000205557.7:p.Leu1066=
ENST00000456970.6:c.3023G>C	ENSP00000405002.2:n.3023G>C
ENST00000622290.4:c.*407G>C	ENSP00000483331.1:n.*407G>C
NM_001171.5:c.3198G>C	NP_001162.4:p.Leu1066=
XM_011522479.1:c.3165G>C	XP_011520781.1:p.Leu1055=
XM_011522480.1:c.2856G>C	XP_011520782.1:p.Leu952=
XM_011522481.1:c.2856G>C	XP_011520783.1:p.Leu952=
XR_932836.1:n.3433G>C
XR_932837.1:n.3434G>C
XR_932838.1:n.3434G>C
NM_001351800.1:c.2856G>C	NP_001338729.1:p.Leu952=
NR_147784.1:n.3060G>C
XM_011522479.2:c.3165G>C	XP_011520781.1:p.Leu1055=
XM_011522481.3:c.2856G>C	XP_011520783.1:p.Leu952=
XM_017023212.1:c.3030G>C	XP_016878701.1:p.Leu1010=
XM_017023214.1:c.3198G>C	XP_016878703.1:p.Leu1066=
XM_024450261.1:c.3234G>C	XP_024306029.1:p.Leu1078=
XR_932836.2:n.3379G>C
XR_932837.3:n.3379G>C
XR_932838.3:n.3379G>C
NM_001171.6:c.3198G>C MANE Select	NP_001162.5:p.Leu1066=